curriculum vitae - biomedical research · curriculum vitae 1. name: robert w. marion, m.d. offices...

CURRICULUM VITAE

1. NAME: ROBERT W. MARION, M.D.

OFFICES Children's Hospital at Montefiore Rose F. Kennedy Center-Rm 237

111 East 210th Street Albert Einstein Col of Med

Bronx, New York 10467 1610 Pelham Pkwy South

Telephone: 718-741-2323 Bronx, New York 10461

FAX: 718-920-6506 Telephone: 718-430-8521

Email: [email protected] FAX: 718-904-1162

2. DATE OF BIRTH: March 27. 1952

Birthplace: Bronx, New York

3. EDUCATION:

1970-1974 Bachelor of Arts Clark University

Worcester, Massachusetts.

1975-1979 Doctor of Medicine Albert Einstein College of Med.,

Bronx, NY

1979-1980 Internship in Pediatrics, Boston Floating Hospital,

Tufts-New England Medical Center,

Boston, MA

1980-1982 Residency in Pediatrics, Bronx Municipal Hospital Ctr/

Einstein Affiliated Hospitals,

Bronx, NY

1982-1984 Postdoctoral Fellowship, Human Genetics,

Genetic Counseling Program,

Einstein, Bronx, NY

ROBERT W. MARION, M.D. PAGE 2

4. PROFESSIONAL APPOINTMENTS:

A. Academic:

mailto:[email protected]

7/1/84-6/30/89 Assistant Professor, Pediatrics,

Albert Einstein College of Medicine,

Bronx, New York.

7/1/89-6/30/94 Associate Professor, Pediatrics,

Albert Einstein College of Medicine,

Bronx, New York.

7/1/94- Professor, Pediatrics

Albert Einstein College of Medicine

7/1/98- Professor, Obstetrics & Gynecology and

Women's Health (secondary)


7/1/96- Adjunct Faculty

Graduate Program in Human Genetics

Sarah Lawrence College

Bronxville, New York

B. Hospital:

7/1/84-6/30/89 Assistant Attending Pediatrician

Bronx Municipal Hospital Center, Bronx, New York.

Jack D. Weiler Hospital of the Albert Einstein

College of Medicine, Bronx, New York.

Montefiore Medical Center, Bronx, New York.

North Central Bronx Hospital, Bronx, New York.

7/1/89-6/30/94 Associate Attending Pediatrician

Bronx Municipal Hospital Center, Bronx, New York


College of Medicine, Bronx, NY

Montefiore Medical Center, Bronx, New York

North Central Bronx Hospital, Bronx, New York


4. PROFESSIONAL APPOINTMENTS (continued)

B. Hospital (continued)

7/1/94- Attending Pediatrician


College of Medicine, Bronx, NY

Montefiore Medical Center, Bronx, New York

Bronx Municipal Hospital Center, Bronx, New York

North Central Bronx Hospital, Bronx, New York

2/1/87- Attending Pediatrician

Blythedale Children's Hospital, Valhalla, New York

C. Administrative

7/1/90-6/30/94 Acting Director, Division of Human Genetics

Department of Pediatrics,

Albert Einstein Col of Med/ Montefiore Med Ctr

Bronx, New York

7/1/90- Director of Medical Genetics

Blythedale Children's Hospital, Valhalla, New York

7/1/94-6/30/02 Director, Division of Genetics


Montefiore Med Ctr/ Albert Einstein Col of Med

Bronx, New York

7/1/02-6/30/04 Co-Chief, Section of Genetics


Children's Hospital at Montefiore/ Albert Einstein

College of Medicine, Bronx, New York

7/1/04 - Chief, Division of Genetics

Department of Pediatrics

Children’s Hospital at Montefiore/Albert Einstein


7/1/97-12/31/02 Consultant in Medical Genetics


Stamford Hospital, Stamford Connecticut.


4. PROFESSIONAL APPOINTMENTS (continued)

C. Administrative (continued)

9/2002- 6/2007 Co-Director, Medical Student Education

Department of Pediatrics, Albert Einstein Col of Med/

Children's Hosp at Montefiore

10/1/06- Chief, Division of Developmental Medicine


Children’s Hospital at Montefiore/Albert Einstein


10/1/06- Director, Children’s Evaluation and Rehabilitation

Center (CERC)

Director, Rose F. Kennedy University Center for

Excellence in Developmental Disabilities

Director, RFK UCEDD LEND Project

Albert Einstein College of Medicine, Bronx, NY

5. MEDICAL LICENSE:

New York State #149231 1984

DEA #AM2454332 1985

NPI #1770669616

6. BOARD CERTIFICATION:

American Board of Pediatrics 1985

American Board of Medical Genetics 1987

7. PROFESSIONAL SOCIETY MEMBERSHIP:

American Society of Human Genetics

American College of Medical Genetics

Association of University Centers in Disabilities (Member, Board of Directors,

November 2008- )

New York State Task Force on Human Genetics (Member, Board

of Directors, 7/1/2002-2006)

New York State Developmental Disabilities Planning Council

Children’s Issues Committee, NYS DDPC

American Society of Professors of Human Genetics

The Authors Guild


8. AWARDS AND HONORS:

1979 Elected to Alpha Omega Alpha,

Einstein Chapter (fourth year medical student)

1979 Upjohn Award for Academic Excellence

(presented to one student in graduating class)

Albert Einstein College of Medicine.

1982 Certificate of Distinction (house officer),

Leo M. Davidoff Society,


1984 Awarded Fraad Fellowship in Child Health,

Department of Pediatrics, Einstein

1991 Christopher Award for The Boy Who Felt No Pain,

(given by the Christopher Society)

1991 The Boy Who Felt No Pain selected for

The Washington Irving Book List,

Westchester County Library Association

1991 Elected to Leo M. Davidoff Society (faculty)


1994 Keynote speaker, Alpha Omega Alpha induction

University of California at Davis Medical School.

1995 Recipient of Sam Rosen Award for outstanding teacher,

preclinical sciences,


(chosen by Einstein students).

1996 Selected as one of "The Best Doctors in America";

American Health Magazine, March, 1996.

1997-2010 Included in "How to Find the Best Doctors: NY Metro Region”


8. AWARDS AND HONORS (continued):

1998 Keynote Speaker, Lori Ann Roscetti Memorial Lecture on

Ethical and Humanitarian Issues in Medicine,

Rush Medical College, Chicago, Ill.

1998-2008, Included in "The Best Doctors in New York";

2010- New York Magazine.

June 2001 Recipient of Lewis Fraad Award for Excellence in Teaching,

Dept of Pediatrics, Einstein (chosen by pediatric house officers)

April 2004 Awarded honorary membership, Men's Division


June 2005 Recipient of the William Obrinsky Award for Excellence in

Medical Student Education, Department of Pediatrics,

CHAM/ Albert Einstein Col of Medicine

June 2006 Honoree at Tenth Annual Awards Dinner, Bronx Mental Retardation

and Developmental Disabilities Council, June 20, 2006

June 2007 Recipient of Lifetime Service Award

Alumni Association of the Albert Einstein College of Medicine

October 2007 Appointed Ruth L. Gottesman Professor of Child Development,


May 2009 Honoree at Spirit of Achievement Luncheon,

National Women’s Division, Albert Einstein College of Med

December 2009 Awarded Zella Bronfman Butler Change Agent Award for 2009

Given by the UJA-Federation of NY & the J.E. and Z.B.

Butler Foundation

November 12, 2010 Honorable Mention Award of the 2010 American Medical Writers

Association Awards, Public Health Care Consumers Category


9. RESPONSIBILITIES AND DUTIES:

A. Clinical

1982-1987 Staff member, Genetic Counseling Program,



1987- Director, Center for Congenital Disorders,

Montefiore Medical Center / EINSTEIN

1987- Medical Director, Einstein Spina Bifida Clinic,

Blythedale Children's Hospital,

Valhalla, New York

1987- Director, Medical Genetics

Blythedale Children's Hospital

Valhalla, New York

2004- Director, Williams Syndrome Center,

Children’s Hospital at Montefiore

Oct. 2006- Medical Director,

Children’s Evaluation and Rehabilitation Center


2007- Co-Director, Einstein/Montefiore Center for NF

Co-Director, Einstein/Montefiore Center for

CardioGenetics

Children’s Hospital at Montefiore/Einstein

. B. Administrative

1987-1990 Pediatric Department representative,

Einstein Student-Faculty Senate

1987- Member, Einstein Admission Committee

1989-1990 Member, Governance council,

Einstein/MMC Pediatric Private Practice

1990 President, Governance Council,

Einstein/MMC Pediatric Private Practice Plan

1990-2002 Member, Executive Policy & Planning Committee

Einstein Dept of Pediatrics (ended in 6/02)


8. RESPONSIBILITIES AND DUTIES (continued):

.

B. Administrative (continued)

1990-2006 Editor-in-chief and founder,

Acta Pediatrica Einsteinia

(Einstein/MMC Pediatric Faculty Newsletter)

1992- Member, Medical Board, Blythedale Children's

Hospital, Valhalla, New York.

1992-1994 Medical Advisory Board,

Save The Children Foundation.

1992-2009 Member, Dean's Select Committee (writer of

Dean's letters), Einstein.

1993-1994 Chairman of ad hoc committees,

1997-1998 Committee on Appointments and Promotions, Einstein.

1993-1994 Medical Advisor, Parents in Partnership, Portland, Maine

1993-2008 Co-Chair, Einstein Committee on Admissions

1994- Member, Committee of Professors

Einstein Dept of Pediatrics

1995-1997 Member, Ethics Committee for Reproductive

Technology, Einstein.

1998 Member, Search Committee for Director of Human

Genetics Program, Sarah Lawrence College,

Bronxville, New York

2005-2006 Chair, Search Committee for Director of CERC

Einstein

2008- Chair, Einstein Committee on Admissions


9. RESPONSIBILITIES AND DUTIES (continued)

C. Educational:

1985-1987 Director, Third Year Student Clerkship in Pediatrics,

Montefiore Med Ctr/North Central Bronx Hosp

1987- Co-director (pediatrics)

Fellowship Program in Medical Genetics; Einstein/MMC

1987- Student Fieldwork Preceptor

Human Genetics Program, Sarah Lawrence College.

1987-1988 Small group leader, Einstein's Introduction to Clinical

Medicine course (first year student course)

1987-1989 Preceptor of third year students,

Pediatric clerkship, Bronx Municipal Hospital Center

1989- Lecturer, senior course in Human Genetics,

Human Genetics Program, Sarah Lawrence College

1990- Lecturer, Einstein's Human Genetics and MCFM Course

for first year medical students.

1996-1998 Member, Division of Education

2002- Albert Einstein College of Medicine.

1997-2001 Course Leader, Introductive to Medicine

2003- Human Genetics Program; Sarah Lawrence College.

2002-2006 Co-Director, Medical Student Education, Dept of Peds,


2002- 2007 Member, Clinical Subcommittee, Division of Education


2002-2006 Member, Task Force of Molecular Medicine in the

Clerkship Years, Division of Education


2003-2006 Member, Division of Education's Scientific Foundations of

Medicine Committee; Einstein


9. RESEARCH/ OTHER SUPPORT:

2007-2012 PI, Rose F. Kennedy University Center for Excellence in Developmental Disabilities

program grant, Administration for Developmental Disabilities of the US Department

of Health and Human Services (total $2.5 M)

2005-2012 PI, Rose F. Kennedy UCEDD LEND Project program grant. Maternal and Child

Health Bureau of HRSA, US Department of Health and Human Services.

(total $3.5 M)

2008-2012 PI: Rose F. Kennedy UCEDD LEND Project, Autism Supplement. Maternal and

Child Health Bureau of HRSA, US Department of Health and Human Services,

(total $800,000)

2008-2011 PI: Feinberg Foundation grant supporting Center for Neurofibromatosis,

(total $500,000)

PI: Jonas Ehrlich Charitable Foundation supporting Autism Research (total

$155,000)

2009-2011 Co-PI, Ethical and Social Implications of Genetic Testing in the Case of Unexpected

Deaths, National Heart, Lung and Blood Institute, (total $915,000).

10. . TRAINEES (POSTDOCTORAL FELLOWS IN MEDICAL GENETICS)

TRAINEE DATE OF DEGREE SCHOOL CURRENT

NAME TRAINING POSITION

Elaine Perreira 7-10 MD Einstein Fellow

Lilian Liu Cohen 7/09- MD Cornell Fellow

Naomi Yachelovich 7/08- MD Fellow

Kathleen Pope 7/07-6/09 MD Maternity Leave

Joy Neil Samanich 7/04-6/06 MD Einstein Ped Genetics

Attending, EINSTEIN

Ann Marie Roe 7/04-6/06 MD Einstein Private Practice


10. TRAINEES (POSTDOCTORAL FELLOWS IN MEDICAL GENETICS) (Cont’d)

Natasha Shur 7/03-6/05 MD Einstein Ass’t Prof

Dept of Peds

Div of Genetics

Brown Univ.

Deborah Barbouth 7/02-6/03 MD U. Argentina Interim Chief

Div of Genetics

Ass’t Prof

Univ of Miami

Susan Klugman 7/02- MD Einstein Chief, Div of

Repro Genetics,

Associate Prof,

Dept of OB/GYN

Einstein

Dwight Cardeiro MD Assistant Prof

Dept of OB/GYN

Harvard Med Sch

Siobhan Dolan 7/01- MD Assistant Prof

Dept of OB/GYN

Div of Repro Gen

EINSTEIN

Robert Soper 7/01 MD St. Luke’s Hosp

Maternal-Fetal

Medicine Att.

Lalaine Mortero 7/97-6/99 MD U Philippines Pediatric Practice Anna Bogdanow 7/94-6/96 MD NY Med Col Retired

Lisa Menasse- 7/93-6/95 MD EINSTEIN Pediatric

Palmer Practice

Jeffrey Karasik 7/91-6/93 MD SUNY-Downstate Pediatric

Practice

Beth Motzkin 7/89-6/91 MD EINSTEIN Clin Genetics

Ellen Stecker 7/87-6/89 MD EINSTEIN Ped Practice


PUBLICATION

A. Original Communications in Reviewed Journals:

1. Chandra P, Nitowsky HM, Marion R, Koenigsberg M, Taben E, Kava HW: Experience with

sonography an adjunct to prenatal diagnosis of fetal genetic disorders. Am J Obst Gynecol

133: 519; 1979.

2. Marion RW: Aganglionic megacolon and cleft palate. J Clin Dysmorphology 1:30, 1983.

2. Goldstein S, Shprintzen R, Wu R, Thorpy M, Hahm S, Marion R, Sher A, Saenger P:

Achondroplasia and obstructive sleep apnea: Correction of apnea and abnormal sleep

entrained growth hormone release by tracheostomy. Birth Defects 21:93; 1985.

4. Marion RW: In the back of the ambulance. JAMA 255: 2654; 1986.

5. Marion RW, Wiznia AA, Hutcheon RG, Rubinstein A: AIDS Embryopathy: A new

dysmorphic syndrome in children with the acquired immune deficiency syndrome. Am J

Dis Child 140: 638; 1986 (Reprinted by the March of Dimes as part of its Professional

Education Reprints series)

6. Marion RW, Wiznia AA, Hutcheon RG, Rubinstein A: Dysmorphism leading to a diagnosis of

AIDS (response to letter). Am J Dis Child 141: 474; 1987.

7. Marion RW, Wiznia AA, Hutcheon RG, Rubinstein A: Fetal AIDS syndrome score:

Correlation between severity of stigmata and age at onset of symptoms of AIDS. Am J Dis

Child 141: 429; 1987.

7a. Marion RW, Wiznia AA, Hutcheon RG, Rubinstein A: Systeme de cotation pour le SIDA

congenital: Correlation entre l'importance de la dysmorphie et l'age au moment du

diagnostic du deficit immunitaire. Am J Dis Child-Journal de Pediatrie 6: 294; 1987

(French translation of 7)

8. Marion R, Alvarez L, Marans Z, Lantos G, Chitayat D: Computed tomography of the brain in

the Smith-Lemli-Opitz syndrome. J Child Neurol 2:198;1987.

9. Marion R, Chitayat D, Hutcheon RG, Shprintzen RJ, Goldberg R, Cohen MM Jr: Autosomal

recessive inheritance in the Setleis bitemporal `forceps mark' syndrome. Am J Dis Child

141:895;1987.


10. Chitayat D, Nakagawa S, Marion R, Sachs GS, Shinnar S, Llena G, Nitowsky HM: Elevation

of serum beta-hexosaminidase and alpha-D-mannosidase in Type 2 Gaucher disease: A

clinical and biochemical study. J Inher Metab Disease 10: 111; 1987.

11. Chitayat D, Hahm S, Marion R, Sachs GS, Goldman D, Hutcheon RG, Cho S, Weiss R,

Nitowsky HM: Further delineation of the McKusick-Kaufman hydrometrocolpos-

polydactyly syndrome. Am J Dis Child 141: 1133; 1987.

12. Goldstein SJ, Wu RHK, Thorpy MJ, Shprintzen RJ, Marion R, Saenger P: Reversibility of

deficient sleep entrained growth hormone secretion in a boy with achondroplasia and

obstructive sleep apnea. Acta Endocrin (Copenh) 116: 95; 1987.

13. Marion RW: A dip in the pool. JAMA 258: 2116; 1987.

14. Wechsler MA, Papa CM, Haberman F, Marion RW: Variable expression in focal dermal

hypoplasia: An example of differential X-chromosome inactivation. Am J Dis Child

142:297; 1988.

15. Marion RW: Explanation for fetal baseline bradycardia in a fetus with panhypopituitarism

and other malformations. Am J Obstet/Gynecol 158:1238; 1988.

16. Marion RW, Chitayat D, Hutcheon RG, Neidich JA, Zackai EH, Singer LP, Warman M:

Trisomy 18 Score: A simple, reliable diagnostic test. J Pediatr 113: 45; 1988.

17. Marion RW: When Tom Died. JAMA 260: 1619; 1988.

18. Farmakides G, Bracero L, Marion R, Fleischer A, Schulman H: Pregnancy termination after

detection of fetal chromosomal or metabolic abnormalities. J Perinatology 8:101;1988.

19. Chitayat D, Nakagawa S, Sachs GS, Marion RW, Sachs GS, Hahm SYE, Goldman HS:

Aspartylglucosaminuria in a Puerto Rican family: Additional features of a panethnic

disorder. Am J Med Genet 31:527;1988.

20. Singer LP, Marion RW, Li JK: Brief clinical report: Limb reduction defects in an infant with

the Smith-Lemli-Opitz syndrome. Am J Med Genetics 32:380,1989.

21. Marion RW: Zebras. Einstein Quart J Biol Med 7:193;1989.

22. Anderson IJ, Marion RW, Goldberg RB, Upholt WB, Tsipouras P: Spondylo-epiphyseal

dysplasia congenita: Evidence for genetic linkage to the COL2A1 locus. Am J Hum

Genet 46:896;1990.


23. Conway EE, Marion RW, Noonan J, Goldberg R, Steeg CN: Myocardial infarction leading to

sudden death in the Williams syndrome: Report of three cases. J Pediatr 117:593-595,

1990.

24. Marion RW, Mayers M: Syndrome identification case report: Facial dysmorphism, growth

and developmental retardation, absence of vocalizations, and other anomalies in two

siblings. Dysmorph Clin Genet 4:149-151, 1990.

25. Chitayat D, Marion RW, Squillante L, Kalousek DK, Das KM: Detection and enumeration of

colonic mucosal cells in amniotic fluid using a colon epithelial specific monoclonal

antibody. Prenatal Diagnosis 10:725;1990.

26. Chhabra R, Suresh BR, Weinberg G, Marion R, Brion LP: Duodenal atresia presenting as

hematemesis in a premature infant with Down syndrome: Case report and review of

the literature. J Perinatology 12:25, 1992.

27. Shprintzen RJ, Goldberg R, Golding-Kushner KJ, Marion RW: Late-onset psychosis in the

velo-cardio-facial syndrome. Am J Med Genet 42:141,1992.

28. Karasik JB, Marion RW, Javed AA: DNA testing for neurofibromatosis, type 1. J Pediatr

121:833,1992.

29. Goldberg R, Motzkin B, Marion R, Scambler PJ, Shprintzen RJ: Velo-cardio-facial

syndrome: A review of 120 patients. Am J Med Genet 45:313, 1993

30. Barone CM, Marion R, Shanske A, Argamaso R, Shprintzen R: Craniofacial, limb and

abdominal abnormalities in a distinct syndrome: Relation to the spectrum of Pfeiffer

syndrome, type 3. Am J Med Genet 45:745, 1993.

31. Marion RW, Garcia D, Karasik JB: Apparent dominant inheritance of Rubinstein-Taybi

syndrome. Am J Med Genetics 46:284,1993.

32. Motzkin B, Goldberg RB, Shprintzen RJ, Marion RW, Saenger P: Variable phenotypes in

velocardiofacial syndrome patients with chromosomal deletions. J Pediatr

123:406,1993.

33. Tavin E, Stecker E, Marion R: Nasal pyriform aperture stenosis and the holoprosencephaly

spectrum. Int J Pediatr Otorhinolaryngology 28:199; 1994

34. Pelayo R, Barasch E, Kang H, Marion R, Moshe SL: Progressively intractable seizures, focal

alopecia and hemimegalencephaly. Neurol 44:969;1994.


35. Glickstein J, Karasik J, Caride DG, Marion RW: "C" trigonocephaly syndrome: Report of a

case with agenesis of the corpus callosum and tetralogy of Fallot and review of the

literature. Am J Med Genet 56:215-218,1995.

36. Chitayat D, Ohel G, Marion R, Einarson TR: Spectrophotometry of amniotic fluid: A simple,

rapid, and inexpensive method for distinguishing between gestational sacs in

midtrimeter amniocentesis for twin pregnancies Obstet/Gynecol 84:569-571,1995.

37. Marion RW: Genetic Drift: The Skeleton in Carl Anderson's Closet. Am J Med Genet 59:1-

4,1995.

38. Marion RW: Genetic Drift: The Unsolved Puzzle. Am J Med Genet 62:327-329, 1996.

39. Marion RW: Genetic Drift: Prying open the box. Am J Med Genet 63:329-331, 1996.

40. Marion RW: Genetic Drift: The Christmas Present. Am J Med Genet 66:247-249, 1996.

41. Bernstein P, Gross SJ, Cohen DJ, Tiller G, Shanske, AL, Bombard AT, Marion RW: Prenatal

diagnosis of Pfeiffer syndrome, type II. Ultrasound Obst Gynecol 8:425-428, 1996.

42. Shanske AL, Bogdanow A, Shprintzen RJ, Lee B, Marion RW: The Marshall syndrome:

Report of a new family and review of the literature. Am J Med Genet 70:52-57,

1997.

43. Shanske AL, Menasse-Palmer L, Caride D, Bogdanow A, Marion RW: Central nervous

system anomalies in the Seckel syndrome: Report of a family and review of the

literature. Am J Med Genet 70:155-158, 1997.

44. Paticoff K, Marion RW, Shprintzen RJ, Shanske AL, Eisig SB: Hemimaxillofacial dysplasia:

A report of two new cases and further delineation of the disorder. Oral Surg, Oral

Med, Oral Pathol 83:484-488, 1997.

45. Quaderi NA, Schweiger S, Gaudenz K, Franco B, Rugarli EI, Berger W, Feldman GJ, Volta

M, Andolfi G, Gilgenkrantz S, Marion RW, Hennekam RCM, Opitz JM, Muenke

M, Ropers HH, Ballabio A: Opitz G/BBB syndrome, a defect of midline

development, is due to mutations in a new RING finger gene on Xp22. Nature

Genetics 17:285-291, 1997.

_


46. Robin NH, Scott JA, Arnold JE, Goldstein JA, Shilling BB, Marion RW, Cohen MM Jr.:

Favorable prognosis for children with Pfeiffer syndrome types 2 and 3:

Implications for classification. Am J Med Genet 75:240-244, 1998.

47. Jacobson Z, Glickstein J, Hensel T, Marion RW: Further delineation of the Opitz G/BBB

syndrome: Report of an infant with complex congenital heart disease and bladder

exstrophy. Am J Med Genet 78:294-299, 1998.

48. Huie ML, Shanske AL, Kasper JS, Marion RW, Hirschhorn R: A large Alu-mediated

deletion, identified by PCR, as the molecular basis for glycogen storage disease,

type II (GSD II). Hum Genet 104:94-98, 1999.

49. Shanske AL, Dowling P, Schmidt R, White BJ, Russell B, Bogdanow A, Marion RW: The

simultaneous occurrence of a r(1) and r(16) in twins. J Med Genet 36:625-628,

1999.

50. Ferreira JC, Carter SM, Bernstein PS, Jabs EW, Glickstein JS, Marion RW, Baergen RN,

Gross SJ: Second trimester molecular prenatal diagnosis of sporadic Apert

syndrome following suspicious ultrasound findings. Ultrasound Obstet Gynecol

14:426-430, 1999.

51. Marion RW: Genetic Drift: Erin, before I knew her. Am J Med Genet 90:95-97, 2000.

52. Schneider EN, Bogdanow A, Goodrich JT, Marion RW, Cohen MM: Fronto-Ocular

Dysplasia: A newly recognized trigonocephaly syndrome. Am J Med Genet 93:89-

93, 2000.

53. Shanske A, Ferreira JC, Leonard JC, Fuller P, Marion RW: Hirschsprung disease in an infant

with a contiguous gene syndrome of chromosome 13. Am J Med Genet 102:231-

236, 2001.

54. Marion RW: Genetic Drift: A Permanent Bond. Am J Med Genet 107:84-86, 2002.

55. Marion RW: Genetic Drift: September 11; 3:00 PM. Am J Med Genet 117:306-308, 2003

56. Dolan S, Gross S, Marion R, Shanske S: First trimester diagnosis of Bartsocas Papas

syndrome by transvaginal ultrasound: Case report and review of the literature.

Prenat Diagn 23:13; 8-142, 2003.


57. Iacoboni D, Karpel BM, Shanske AL, Marion RW, Gross SJ: Prenatal diagnosis of

Marshall syndrome by targeted sonography. J Ultrasound Med 24 (12); 1735-1737, 2005.

58. Shur N, Marion R, Gross SJ: A surprising postnatal diagnosis. Obstet Gynecol 108:189-195, 2006,

59. Polotsky A, Shur N, Marion R: A flat head in a round world: Dispelling common myths about

plagiocephaly. The Female Patient 32:46-48, 2007.

60. Marion RW: Two miracles, one year later. Am J Med Genetics Part C Semin Med Genet 151C:

167-172, 2009.

61. Hatchel A, Willis J, Reiser C, Marion R, Pariseau C, Vanner-Nicely L, Bodurtha J. Diversity in

genetic counseling: strategies from the LEND network. J Genet Couns. 2009; 18(2):195-6.

62. Cohen LL, Samanich J, Marion RW: 17q12 Deletion in a Williams Syndrome Patient: Case Report

and Review of the Literature. J Ped Genet (in press)

63. Pereira EM, Marion R, Ramesh KH, Kim J, Ewart M, Ricafort R: Brief Report: Hepatoblastoma in a

mosaic type trisomy 18 patient. (submitted to Pediatric Blood and Cancer)

64. Erskine KE, Griffith E, DeGroat N,Stolerman M, Silverstein LB, Hidayatallah N, Wasserman,

D, Paljevic E, Cohen L,Walsh CA, McDonald TV, Marion RW, Dolan SM: An

Interdisciplinary Approach to Personalized Medicine: Case Studies from a Cardiogenetics

Clinic. Genetics in Medicine (submitted).

65. Marion RW, Shanske AL, Levy P, Shprintzen RJ: The Shprintzen-Goldberg syndrome: Report

of half siblings and review of the literature (submitted to Am J Med Genet).

B. Books, Chapters in Books, and Review Articles:

1. Marion, Robert: Born Too Soon_(a novel) New York: Doubleday and Company; Oct, 1985.

1a. Marion, Robert: Born Too Soon.(a novel). London:Robert Hale, 1986.

2. Marion R: Mononucleosis. In Handbook of Pediatric Emergency Therapeutics_, Crain E and

Gershel J, eds. New York: Appleton-Century-Crofts , December, 1985.

3. Marion R: Kawasaki Disease. In Handbook of Pediatric Emergency Therapeutics, Crain E

and Gershel J, eds. New York: Appleton-Century-Crofts, December, 1985.

4. Marion RW: Fetal AIDS syndrome. In Nebraska Perinatal Letter, vol 2,November, 1987, p 8.

5. Marion R: Neural tube defects: Meningomyelocoele and anencephaly. In Fahn S ed, Current

Opinions in Neurology and Neurosurgery, 1:353-357;1988.


6. Marion R: In the Back of the Ambulance. In Dan BB and Young RK (eds): A Piece of My

Mind_. Los Angeles: Feeling Fine Press, 1988; p 165.

7. Marion R: A Dip in the Pool. In Dan BB and Young RK (eds):A Piece of My Mind. LA:

Feeling Fine Press, 1988; p 214.

8. Marion, Robert: The Intern Blues: The Private Ordeals of Three Young Doctors. NY:

William Morrow & Co, 1989.

8a. Marion, Robert: The Intern Blues: The Private Ordeals of Three Young Doctors

(paperback edition). NY: Fawcett Crest Publishing Company; August, 1990.

8b. Marion, Robert: The Intern Blues: The Timeless Classic About the Making of a Doctor.

New York: HarperPerrenial, 2001.

9. Marion, RW: Book Review: Metabolic Basis of Inherited Disease, Sixth Edition, edited by

Scriver, Beaudet, Sly and Valle. Einstein Quart J Biol Med 7:196; 1989.

10. Marion RW, Chambers P, Schendel L: Meningomyelocoele. In Johnson RT (ed): Current

Therapy in Neurologic Disease. Philadelphia: BC Decker, Inc, p 85; 1990.

11. Marion R: Alex Goes for a Walk. In Reader's Digest, September, 1990; pp 54-58.

12 Marion RW: The Boy Who Felt No Pain. New York: Addison-Wesley Publishing Company,

September, 1990.

12a. Marion RW: De Mooiste Ogen Van de Wereld, en andere verhalen van een kinderarts.

(Dutch language version of The Boy Who Felt No Pain) Amsterdam: Prometheus,

February, 1991.

12b. Marion RW: Das Kind, das keinen Schmerz fuehlen konnte (German language version of

The Boy Who Felt No Pain). Munich, Germany: R. Piper Publishing Co., 1992.

12c. Marion RW: The Boy Who Felt No Pain (paperback edition). New York: Fawcett Crest

Publishers, 1991.

13. Rosa FW, Marion RW, Wiznia AA, Qazi Q: Fetal AIDS infection. In Buyse ML (ed): Birth

Defects Encyclopedia. New York: Alan R. Liss, Inc., 1990, p 682.

14. Torielo H, Marion RW: Ectodermal dysplasia, congenital facial, Setleis type. In Buyse ML

(ed): Birth Defects Encyclopedia. New York: Alan R. Liss, Inc, 1990, p 598.

15. Marion R: The Mystery of Cassandra. In the Saturday Evening Post, Jan-Feb, 1991, pp 26-

27, 92-96.


16. Marion RW: Commentary on "de Myer sequence" by Spolyar et al. Cleft Palate J

28:113,1991.

17. Marion R: Birth Defects. In Shelov SP ed, American Academy of Pediatrics' Book of

Baby and Child Care- Birth to Age Five. 1991.

18. Marion R: In Memoriam: Lewis M. Fraad (1907-1990): Proceedings of memorial service.

Einstein Quart J Biol Med 9:33, 1991.

19. Marion RW: Genetic Anatomy of Hearing: A Clinician's View. In Ruben RJ, van de Water

R, Steel KP (eds): Genetics of Hearing Impairment, Ann NY Acad Science

630:32-37,1991.

20. Marion RW and Fleischman, AR: The Assessment and Management of Neonates With

Congenital Anomalies. In Evans, M, ed: Reproductive Risks and Prenatal

Diagnosis_. Norwalk, CT: Appleton, Lange, 1992, pp 341-358.

21. Marion RW: Learning to Play God: The Coming of Age of aYoung Doctor. NY:

Addison-Wesley Pub Company, 1991.

21a. Marion RW: Learning to Play God: The Coming of Age of a Young Doctor_ (condensed

version). In Today's Best Nonfiction. Pleasantville, NY: Reader's Digest

Association, 1992.

21b. Marion RW: Learning to Play God: The Coming of Age of aYoung Doctor (paperback

edition). NY: Fawcett Crest, 1993.

21c. Marion RW: Learning to Play God (paperbook). NY: Fawcett Publishing Co, 2000.

21d. Marion RW: Im Dienst des Lebens: Meine Anfangsjahre als Arzt (German language

version of Learning to Play God). In Im Spiegel der Zeit: Das Beste. Stuttgart,

Germany: Reader's Digest, 1995.

22. Marion R, Schneider M: The Approach to the Adolescent with a Genetic Disorder. In

Friedman SB, Fisher M, Schonberg SK (eds): Comprehensive Adolescent Health

Care_; St. Louis, Mo: Quality Medical Publishing 1992, pp 603-624.

22a. Marion R, Schneider M: The Approach to the Adolescent with a Genetic Disorder. In

Friedman SB, Fisher M, Schonberg SK (eds): Comprehensive Adolescent Health

Care; 2nd Edition_; St. Louis: Quality Medical Publishing 1997, pp .


22b. Marion R, Schneider M: Chapter 148: Genetic Disorders. In

Rosenberg W, Alderman E, Fisher M (eds): AAP’s Textbook of Adolescent Health

Care; 3rd Edition_; Elk Grove Village, Il: American Academy of Pediatrics (in

press).

23. Marion R: Life and Death 101. Physician (Montefiore Medical Center) Spring, 1992:12-13.

24. Marion R: Doctor to doctor: Following an intern through his first month. Career Insights

M.D. Summer, 1992:30-32.

25. Marion RW: Table: Genetic Emergencies. In Crain EF, Gershel JC, and Gallagher EJ (eds):

Handbook of Pediatric Emergency Therapeutics, 2nd edition, NY: Appleton-

Century-Crofts 1992, pp 187-192.

25a. Marion RW: Genetic Emergencies (second edition). In Crain EF, Gershel JC, and

Gallagher EJ (eds): Clinical Manual of Emergency Pediatrics, third edition.

NY: McGraw Hill, 1996, pp 249-254.

25b. Marion RW: Genetic Emergencies (third edition). In Crain EF, Gerschel JC, and Gallagher

EJ (eds): Clinical Manual of Emergency Pediatrics, fourth edition. NY:

McGraw Hill, 2003, pp 253-256.

25c. Marion RW: Genetic Emergencies (fourth edition). In Crain EF, Gerschel JC, and Gallagher

EJ (eds): Clinical Manual of Emergency Pediatrics, fifth edition. NY:

Cambridge Press (in press).

26. Marion RW: Andrew's parents. Hippocrates, February,1993, pp 24.

27. Marion RW: Syndromes associated with vaginal and uterine malformations. In Tenenbaum

S (ed): Dialogues in Pediatric Urol 16;6,1993.

28. Marion, RW: Why the father of our country was childless. New York Newsday, Monday,

February 21, 1994, p 34.

29. Marion R: Was George Washington Really the Father of our Country? A Clinical

Geneticist Looks at World History. New York: Addison-Wesley Publishing Co,

February, 1994.

30. Marion RW: Kevin's Question. In Ladies Home Journal's Parent Digest, Fall/Winter,

1994, pp 30-33.


31. Marion RW: Foreward: What Doctors Think Patients Want From Their Doctors. In Bowman

P, Grady M, Kendrick M, Ladew-Duncan J, Mentzer S, Newman R, Pease R, Son K,

Spadinger L: From the Heart: Stories by Mothers of Children With Special

Needs_. Portland, Me: U Southern Maine Press, 1994, pp xii-xx.

32. Marion RW: Craniosynostosis. Pediatr Rev 16:115-116, 1995.

33. Marion RW: Vital Signs: The Girl Who Mewed. Discover magazine, August, 1995, pp 38-

40.

34. Bogdanow A, Menasse-Palmer L, Shanske AL, Marion RW: Cleft palate. Ped Rev 16:425-

426, 1995.

35. Menasse-Palmer L, Bogdanow A, Marion RW: Choanal atresia. Pediatr Rev 1995, 16:475-

476.

36. Marion RW: Vital Signs: A Cry from the Brain. Discover magazine. December 1995, pp 42-

46.

37 Marion RW: Chapter 21: Genetics. In Shelov SP and Bernstein D (eds): Pediatrics for

Medical Students. Baltimore, MD: Williams and Wilkins, 1996, pp 417-436.

37a. Marion RW: Chapter 11: Genetics. In Bernstein D and Shelov SP (eds): Pediatrics for

Medical Students, 2nd

edition. Media PA: Lippincott Williams & Wilkins, 2003,

pp. 227-246.

37c. Marion RW and Samanich JN: Chapter 11: Genetics. In Bernstein D and Shelov S (eds):

Pediatrics for Medical Students, 3rd

Edition. Philadelphia: Lippincott, Williams

and Wilkins, 2012, pp 251-273.

38. Marion RW: Umbilical anomalies. In Hoekelman RA (ed): Primary Pediatric Care, 3rd

Edition. St. Louis, MO: Mosby-Year Book, Inc, 1996, pp .

38a. Marion RW: Chapter 268: Umbilical Anomalies. In Hoekelman RA (ed): Primary

Pediatric Care, 4th Edition_. St Louis, MO: Mosby-Year Book, Inc, 2001, pp

38b. Samanich J, Marion RW: Umbilical Anomalies. In Hoekelman RA (ed): Primary Care

Pediatric Care, 5th

Edition. St. Louis, MO: Mosby-Year Book, Inc (in press)

39. Marion RW: Halloween. In Sachs D (ed): Emergency Room: Lives Saved and Lost:

Doctors Tell Their Stories. Boston: Little Brown, 1996, pp 179-183.


40. Marion RW: Vital Signs: Andrew of the Dark. Discover magazine, February, 1997, pp. 36-

39.

41. Marion RW: Rotations: The Twelve Months of Intern Life. New York: Harper Collins

Publ Co, 1997.

41a. Marion RW: Rotations: The Twelve Months of Intern Life (paperback edition). New

York: Harper Collins Publ Co, June, 1998.

41b. Marion RW: Rotations: The Twelve Months of Intern Life (Japanese editions) Nishimura

Company LTD, 2004.

42. Marion RW: What the well-dressed house officer will be wearing this season. In E=MD2

(Alumni magazine of Albert Einstein College of Medicine), Spring, 1998.

43. Marion RW: Vital Signs: The baby who stopped eating. Discover magazine, August, 1998,

pp 42-45.

43a. Marion R: The baby who stopped eating. In Alcamo IE (ed): Encounters in Microbiology.

Boston: Jones & Bartlett Publishers, 2001, pp 53-60.

44. Marion RW: Vital Signs: A case of abuse. Discover magazine, September, 1999, pp 44-49.

45. Marion RW: Vital Signs: The curse of the Garcias. Discover magazine, December, 2000, pp

42-46.

46. Marion RW: Growing old quickly in the Bronx. E=MD2: The Alumni Magazine of the Albert

Einstein College of Medicine, Fall, 2003,

47. Levy P and Marion RW: Section IX: Human Genetics and Dysmorphology; Chapter

47: Patterns of Inheritance; Chapter 48: Genetic Assessment; Chapter 49: Chromosomal

Disorders; Chapter 50: The Approach to the Dysmorphic Child. In Kliegman RM,

Marcdante KJ, Jenson HB and Behrman RE (eds), Nelson's Essentials of Pediatrics, Fifth

Edition. Philadelphia, pp. .

47a. Levy P and Marion RW: Section IX: Human Genetics and Dysmorphology;

Chapter 47: Patterns of Inheritance;

Chapter 48: Genetic Assessment;

Chapter 49: Chromosomal Disorders;

Chapter 50: The Approach to the Dysmorphic Child.

In Marcdante KJ, Kliegman RM, Jenson HB and Behrman RE (eds), Nelson's Essentials of

Pediatrics, Sixth Edition. Philadelphia: Elsevier Saunders, 2010, pp 167-186.


48. Marion R: Two Miracles, One Year Later. E=MD2 (EINSTEIN Alumni Magazine) Summer

2006, pp. 20-25.

49. Marion R: Review of The Soul of A Doctor: Harvard Medical Students Face Life and

Death. Diversion magazine, June 2006.

50. Dolan S, Marion R: Sociocultural aspects of working with a family affected with a rare

autosomal recessive condition. In Silberman S, Correa N, Strelnick AH, Townsend J and

Spano H (eds): Teaching Cases Exploring Cross-Cultural Care. New York: Bronx

CREED, 2007.

51. Rosen O, Marion R: Chapter: Common Congenital Anomalies Detected in the Neonatal

Period: Approach and Diagnosis. In Hoekelman RA (ed): Primary Care Pediatrics,

5th

Edition. St. Louis, MO: Mosby-Year Book, Inc (in press).

52. Samanich J, Marion R: Chapter: Dysmorphology. In Hoekelman RA (ed): Primary Care

Pediatrics, 5th

Edition. St. Louis, MO: Mosby-Year Book, Inc (in press).

53. Marion R: Oral Manifestations of Genetic and Congenital Disorders. In Robbins M and

Romer M, (eds): Special Care Dentistry for the General Practice Resident: Practical

Training Modules. NYS Office of Mental Retardation and Developmental Disabilities.

54. Marion RW: Genetic Round: A Doctor’s Encounters in the Field That Revolutionized Medicine.

New York: Kaplan Publishing Company, Oct 2009.

54a. Marion RW: Genetic Rounds: A Doctor’s Encounter in the Field That Revolutionized

Medicine. Paperback edition. New York: Kaplan Publishing Company, Dec. 2010.

55. Marion RW: Autism Spectrum Disorder and the Clinical Geneticist: An Approach to the Family.

In Autism Spectrum News, Volume 2 No. 1, Summer 2009, p 31.

56. Marion RW: Einstein Editions: Genetic Rounds: A Doctor’s Encounters in the Field that

Revolutionized Medicine. Einstein: The Magazine for Alumni and Friends of the Albert Einstein

College of Medicine of Yeshiva University. Winter/Spring 2010, pp 20-23.

57. Marion Robert: Personalized Medicine: The Future is Now – or at least very soon. HealthWorks:

Medicine, Prevention, Wellness. The Journal News, June 2010, pp 8-10.


C. Abstracts:

1. Nitowsky HM, Koenigsberg M, Marion R, Macri J: Maternal alpha-fetoprotein (AFP) before

and after amniocentesis and correlation with sonography findings. Am J Hum

Genetics 117:182S; 1980 (presented at poster session, American Soc Hum Genetics

Meeting, New York, October 1980).

2. Marion RW, Nitowsky HM: Association of advanced parental age with the Prader-Willi

syndrome. Pediatr Res 16:193A; 1982 (presented at a poster session, APS-SPR

annual meeting, Washington, D.C., May 1982).

3. Hahm S, Marion RW, Schwartz G, Nitowsky HM: Failure to thrive: a manifestation of

Klinefelter syndrome. Pediatr Res 16:192A; 1982.

4. Marion RW, Nitowsky HM, Ben-Yishay M, Goldman D: Unexpected pregnancy outcome

following midtrimester amniocentesis. Pediatr Res 17:214A;1983.

5. Nakagawa S, Kumin S, Nitowsky HM, Marion R: A variant of hexosaminidase A (Hex A)

deficiency in Ashkenazi Jews. Pediatr Res 17:216A, 1983.

6. Marion RW, Nitowsky HM: Demonstration and significance of heterogeneity in the etiology of

dark amniotic fluid. Am J Hum Genetics 36:194S;1984 (presented at a poster

session, Am Soc Human Genetics annual meeting, October, 1984).

7. Marion RW: Correlation between parietal hair whorl location and brain dominance. Pediatr

Res 19:328A; 1985 (presented at a poster session, APS/SPR/APA mtg, Washington

DC, 4/85).

8. Goldberg R, Marion R, Borderon M, Wiznia A, Shprintzen RJ: Phenotypic overlap between

velo-cardio-facial syndrome and the diGeorge sequence. Am J Human Genetics

37:A54, 1985.

9. Shprintzen RJ, Wang F, Goldberg R, Marion R: The expanded velo-cardio-facial syndrome:

Additional features of the most common clefting syndrome. Am J Human Genetics

37: A77, 1985 (presented at a poster session, Am Soc Human Genetics annual

meeting, October, 1985.)

10. Marion R, Wiznia A, Hutcheon RG, Rubinstein A: The AIDS Embryopathy: A new

dysmorphic syndrome in children with acquired immune deficiency syndrome.

Pediatr Research 20:339A, 1986 (presented at plenary session, APS-SPR

annual meeting, Washington, D.C., May 4, 1986.)


11. Marion R. Wiznia A, Hutcheon RG, Rubinstein A: HTLV-III Embryopathy score:

Correlation between severity of dysmorphism and age at onset of immune

deficiency. Am J Hum Genetics 39: A70, 1986 (presented at slide session,

Am Soc Human Genetics annual meeting, Philadelphia, Nov, 1986).

12. Chitayat D, Hahm S, Marion R, Hutcheon G, Sachs G, Goldman D, Weiss R, Cho S: Further

delineation of the McKusick-Kaufman Hydrometrocolpos-Polydactyly syndrome.

Am J Human Genetics 39; A56, 1986 (presented at poster session, Am Soc Hum

Genetics annual meeting, Philadelphia, PA, November, 1986).

13. Nakagawa S, Chitayat D, Marion R, Sachs G, Shinnar S, Nitowsky HM: Elevated beta-

hexosaminidase and alpha-D-mannosidase in Type I Gaucher disease: A clinical and

biochemical study. Am J Human Genetics 39; A16, 1986 (presented at a poster

session, Am Soc Hum Genetics annual meeting, Philadelphia, PA, November,

1986).

14. Wiznia AA, Marion RW, Hutcheon RG, Campbell D, Calvelli T, Rubinstein A: Prediction of

HIV seropositivity in a newborn and mother based on features of the fetal AIDS

syndrome in the child. Pediatr Research 21: 211A; 1987.

15. Diamond G, Marion RW, Wiznia AA, Belman A, Cohen HJ, Rubinstein A: Dizygotic twins

discordant for HIV infection: A multidisciplinary study. Pediatr Research

21: 422A; 1987.

16. Marion RW, Wiznia AA, Shah K, Rubinstein A: Fetal AIDS syndrome: Lack of correlation

with maternal drug use. III International Congress on AIDS Abstracts Volume, 135,

1987 (presented at a poster session, III International Congress on AIDS, June 3,

1987).

17. Marion RW, Chitayat DA, Hutcheon RG, Neidich J, Warman M: Trisomy 18 score: A

reliable clinical test for trisomy 18. Am J Human Genetics 41: A74; 1987.

(presented at a poster session, Am Soc Human Genetics annual meeting, San Diego,

Ca, 10/8/87).

18. Nakagawa S, Chitayat DA, Marion RW, Sachs GS, Hahm SYE, Goldman HS, Nitowsky HM:

Aspartylglucosaminuria in a Puerto Rican family: Additional features of a pan-

ethnic disorder. Am J Human Genetics 41: A13; 1987.

19. Wechsler M, Papa C, Haberman B, Marion RW: Variable expression in focal dermal

hypoplasia: An example of "unfavorable Lyonization"?. Am J Human Genetics 41:

A89; 1987. (presented at a poster session, Am Soc Hum Genet annual meeting, San

Diego Ca, 10/7/87).


20. Marion RW, Wiznia AA, Lyman WD, Kashkin J, Rubinstein A: Is the HIV embryopathy

caused by abnormal development of neural crest cells? Pediatr Res 23:269A, 1988.

21. Das K, Chitayat DA, Marion RW: Detection and enumeration of colonic mucosal cells in

amniotic fluid using a cell-specific monoclonal antibody. Am J Human Genetics

41:A272; 1987. (presented at poster session, Am Soc Human Genetics annual

meeting, San Diego, Ca, 10/7/87).

22. Wiznia A, Marion R, Hutcheon G, Rubinstein A: Further delineation of the HIV

embryopathy. IV International Congress on AIDS, Abstract Volume 1988.

23. Conway EE, Marion RW, Goldberg R, Steeg CN, Mitsudo S: Myocardial infarction in the

Williams syndrome: A cause of sudden death. Am J Hum Genet 43:A44,1988.

24. Marion RW. Wiznia AA, Hutcheon RG, Rubinstein A: Further delineation of the HIV

Embryopathy. Am J Human Genetics 43:A60,1988.

25. Anderson IJ, Marion RW, Goldberg RB, Upholt WB, Tsipouras P: Spondyloepiphyseal

dysplasia congenita: Evidence for genetic linkage to the COL2A1 locus.

Pediatr Research 25:138A,1989. (presented at platform slide session, SPR/APS

annual meeting, Washington, DC, May, 1989).

26. Marion R, Goldberg R, Young R, Jorgenson R, Shprintzen R, Shroer R: The GRANDDAD

syndrome: A disorder combining growth delay, "aged facies," normal development,

and deficiency of subcutaneous fat. Am J Human Genetics 45: A53; 1989

(presented at poster session, American Soc Hum Genetics meeting, Nov, 1989).

27. Schwartz RC, Watkins D, Fryer AE, Goldberg R, Marion R, Polomeno RC, Spallone A,

Upadhyaya M, Harper P, Tsipouras P: Non-allelic genetic heterogeneity in the

vitreoretinal degenerations of the Stickler and Wagner types and evidence for

intragenic recombinations at the COL2A1 locus. Am J Hum Genet 45: A219; 1989

(presented at platform slide session, American Soc Hum Genetics meeting,

November, 1989).

28. Goldberg RB, Marion RW, Pritzker H, Wang F, Anderson I, Tsipouras P:

Spondyloepiphyseal dysplasia congenita: Evidence of variability of expression in a

large family. Am J Human Genetics 45:A46; 1989 (presented at platform slide

session, Am Soc Hum Genet meeting, November, 1989).

29. Paulson C, Mann E. Rabin A, Marion R, Nitowsky H, Schmidt R: Premature centromeric

separation in an obligate heterozygote for Roberts-SC phocomelia syndrome. Am J

Hum Genet 45: A87; 1989 (presented at poster session, American Soc Hum

Genetics meeting, November, 1989)


30. Marion RW, Motzkin BA, Neidich JA, Davis JG, Traeger EC: Long-term survival in the

Jarcho-Levin syndrome is related to lack of respiratory distress in the newborn

period. Am J Human Genetics 47:A66,1990.

31. Conway EE, Noonan J, Marion RW, Steeg CN: Myocardial infarction leading to sudden

death in the Williams syndrome: Report of three cases. Am J Hum Genet

47:A52,1990 (presented at poster session, Am Soc Hum Genetics meeting,

Cincinatti, Ohio, October, 1990).

32. Motzkin BA, Goldberg R, Wechsler M, Marion RW: Brain imaging in variants of the

holoprosencephaly malformation sequence: The face is the best predictor of the

brain. Am J Human Genetics 47:A68,1990.

33. Marion RW, Marzullo L, Stein JHR, Goldberg R, Schendel L, Brown R, Schaefer D:

Prognostic indicators of developmental outcome in infants with meningomyelocele.

Am J Hum Genet 49 (supp):149; 1991. (presented at poster session, 8th International

Cong of Human Genetics, Washington, DC, Oct, 1991)

34. Goldberg RB, Shprintzen RJ, Marion RW, Guthrie E: Late onset psychosis in the

velocardiofacial syndrome. Am J Human Genetics 49 (supp):312;1991 (presented at

poster session, 8th International Congress of Human Genetics meeting, Washington,

DC, October 7, 1991).

35. Motzkin B, Goldberg R, Shprintzen R, Marion R, Saenger P: Variable phenotypes in

velocardiofacial patients with chromosomal deletions. Pediatr Res 31:70A,1992

(presented at platform slide session, SPR/APS meeting, Baltimore, MD, April,

1992).

36. Karasik JB, Garcia DM, Pritzker H, Marion RW: Deletion of 1q21q24 in a patient with

features of microcephalic osteodysplastic primordial dwarfism, type II. Am J

Human Genet 51;A82,1992 (presented at poster session, American Society of

Human Genetics, San Francisco, Nov 11, 1992).

37. Garcia D, Karasik J, Marion R: Apparent dominant transmission of Rubinstein-Taybi

syndrome. Am J Human Genet 51;A95,1992 (presented at poster session, American

Soc of Human Genetics Annual Meeting, San Francisco, CA, November 12, 1992).

38. Marion R, Garcia D, Karasik J: Apparent dominant transmission of Hallermann-Streiff

syndrome. Am J Hum Genet 51;A102,1992 (presented at poster session, Am Soc of

Human Genetics, San Francisco, November 10, 1992).


39. Dowling PK, Marion RW, Lesser ES, Schmidt R: A dicentric marker chromosome [inv

dup(15)(pterq11.2:;q11.2pter)] associated with perinatal leukemoid reaction and

situs inversus totalis. Am J Human Genet 51; A288, 1992.

40. Pelayo R, Barasch E, Kang H, Marion R, Moshe SL: Progressively intractable seizures and

alopecia. (Presented at the 46th Annual Eastern Association of

Electroencephalographers, Dec 3, 1992, NY, NY).

41. Marion RW: Did Napoleon have the late-onset form of 17-ketosteroid reductase deficiency?

Am J Hum Genet 52;A , 1993.

42. Salomon M, Ramaswamy P, Garcia D, Marion RW: Hyperthermia as a complication of

Prader-Willi syndrome: Report of 2 additional patients. Am J Hum Genet 52;A ,

1993. (presented at a poster session, Am Soc Hum Genet, New Orleans, La.,

October 4, 1993).

43. Marion R, Shanske A, Goldberg R, Sicklick M, Wiznia A, Shprintzen R: Prevalence of

immune dysfunction in velo-cardio-facial syndrome. Am J Med Genet 1994.

(presented at a platform slide session, Am Col Med Genet, 1st Annual Meeting,

Kissimmee, FL, March 16, 1994).

44. Dorf SB, Caride DG, Schendel L, Marion RW: Factors determining decision to have

subsequent children after the birth of a child with spina bifida in an inner city

population. Am J Hum Genet 54; A141; 1994. (presented at poster session, Am

Soc of Hum Genetics annual meeting, Montreal, Canada, October 16, 1994).

45. Menasse-Palmer L, Leo J, Cannizaro L, Parnes B, Glickstein J, Shanske A, Marion R: Partial

trisomy 14q and monosomy 20q due to an unbalanced familial translocation. Am J

Hum Genet 54: A320; 1994.

46. Rosenberg R, Greenhill K, Marion RW, Brown WT, Jenkins E: Unexpectedly low incidence

of fragile X syndrome in a developmentally disabled inner city population. Am J

Hum Genet 54: A116; 1994. (presented at poster session, Am Soc Hum Genet

annual meeting, Montreal, Canada, Oct. 16, 1994).

47. Bogdanow A, Menasse-Palmer L, Lesser I, Levy P, Marion R: Association between Russell-

Silver syndrome and attention deficit-hyperactivity disorder and/or learning

disabilities: Report of 16 cases. Am J Hum Genet 57: A84, 1995 (presented at

poster session, American Soc of Human Genetics meetings, Minneapolis, 10/95).

48. Eisig S, Marion R, Shprintzen R, Shanske AL: Hemimaxillofacial dysplasia: A report of 2

new cases and further delineation of the disorder. Am J Hum Genet 57: A88,

1995. (presented at poster session, American Society of Human Genetics meetings,

Minneapolis, Oct, 1995).


49. Kim ES, Bogdanow A, Menasse-Palmer L, Marion R, Shanske AL: Cystic hygroma and

massive hydrops in a 45,X fetus with obstructive uropathy. Am J Hum Genet 57:

A310, 1995.

50. Menasse-Palmer L, Bogdanow A, Hantman E, Pritzker H, Marion R: Further delineation of

acromesomelic dysplasia: Report of 2 cases. Am J Hum Genet 57: A97, 1995

(presented at poster session, Am Soc Hum Genet meetings, Minneapolis, Oct, 1995).

51. Shprintzen RJ, Shanske AL, Marion RW, Goldberg R: The expansive phenotype of velo-

cardio-facial syndrome: A review of 206 cases. Am J Human Genet 59: A20, 1996.

(presented at platform slide session, American Society of Human Genetics annual

meeting, San Francisco, CA, October 31, 1996.

52. Robin NH, Scott JA, Arnold JE, Goldstein JA, Shilling BB, Marion R, Muencke M, Cohen

MM: A better than expected developmental outcome in Pfeiffer syndrome type 3.

Am J Med Genet 59: A36, 1996 (presented at platform slide session, Am Soc

Human Genetics annual meeting, Nov 1, 1996, San Francisco, CA.)

53. Dowling P, Schmidt, White BJ, Russell B, Marion R, Cazano C, Salem M, Shanske A: The

simultaneous occurrence of a r(1) and a r(16) in twins. Am J Hum Genet 59:A116,

1996 (presented at poster session, Am Soc Human Genetics meeting, San

Francisco, CA, October, 1996).

54. Marion RW, Schendel L, Caride DG, Cardeiro DJ, Bogdanow A: Mortality and outcome in

children with myelomeningocele: A 10 year experience. Am J Hum Genet

59:A169, 1996 (presented at poster session, Am Soc Human Genetics annual

meeting, San Francisco, CA, October, 1996).

55. Bernstein P, Gross SJ, Cohen DJ, Tiller GR, Shanske AL, Bombard AT, Marion RW: Prenatal

diagnosis of Pfeiffer syndrome, type 2. Am J Hum Genet 59: A317, 1996

(presented at poster session, Am Soc Human Genetics annual meeting, San

Francisco, CA, October, 1996).

56. Bogdanow A, Goodrich J, Hantman E, Shanske A, Marion R: A new autosomal dominant

trigonocephaly syndrome with dysmorphic facies and congenital heart disease. Am

J Hum Genet 59: A348, 1996.

57. Soper R, Gross SJ, Kutcher R, Kim ES, Caride D, Marion RW: Prenatal diagnosis of cerebro-

oculo-facio-skeletal syndrome.(presented at poster session, American Institute of

Ultrasound in Medicine annual meeting, San Diego, Ca, March, 1997).


58. Seiff M, Keating R, Seimon L, Marion R, Goodrich J: Long term outcome in

myelomeningocele: These kids are doing better than you think (presented at the

annual meeting of the American Association of Neurological Surgeon,

November, 1996).

59. Mbekeani JN et al.: Bilateral iris hypoplasia associated with cardiovascular and urogenital

anomalies: A new autosomal dominantly inherited syndrome? (presented at

the annual meeting of the American Acad of Ophthalm)

60. Jacobson Z, Glickstein J, Hensel T, Marion RW: Further delineation of the Opitz G/BBB

syndrome: Report of a child with complex congenital heart disease and bladder

exstrophy. Am J Hum Genet 61:A102, 1997 (presented at poster session, Am Soc

Hum Genet annual meeting, Baltimore, Maryland, October 30, 1997).

61. Ferreira J, Ben-Yishay M, Gross SJ, Pulijaal V, Gogineni, Nitowsky HM, Morrow B,

Goldberg R, Marion R: Prenatal diagnosis of familial velocardiofacial syndrome:

Clinical and counseling issues. Am J Hum Genet 61:A152, 1997 (presented at poster

session, Am Soc Hum Genet annual meeting, Baltimore, Oct 30, 1997).

62. Kramer L, Levy P, Bogdanow A, Hantman E, Marion R: Presenting features in the

mucopolysaccharidoses: A review of 12 consecutive cases. Am J Hum

Genet:A395,1997.

63. Sylvestre G, McDermott DA, Carter SM, Pulijaal VR, Marion RW, Gross SJ: Expansion of

the mosaic trisomy 15 phenotype in a liveborn infant: clinical and cytogenetic study.

Am J Human Genet 63:A122, 1998 (presented at a poster session, American Society

of Human Genetics annual meeting, Denver, Colorado, October, 1998).

63. Marion RW, Rojas BM, Romanowitz H, Lasley LK, Borras L, Mate-Kole J, Powell S, Sadek

K, Caine E: Unbalanced autosomal chromosomal translocation carried by mosaic

mother ofaffected offspring. Am J Hum Genet 63:A144, 1998 (presented at poster

session, Am Soc Hum Genet annual meeting, Denver, Colorado, Oct, 1998).

64. Huie ML, Kasper JS, Shanske AL, Marion RW, Hirschhorn R: A large (9kb) Alu mediated

deletion extending past the 3' end of the gene in Glycogen Storage Disease Type II.

Am J Hum Genet Am J Hum Genet 63:A365, 1998 (presented at poster session, Am

Soc Hum Genet annual meeting, Denver, Colorado, Oct, 1998).

65. Shanske AL, Ferreira JC, Attiyeh E, Marion RW: Hirschsprung disease in an infant with a

contiguous gene syndrome of chromosome 13. Pediatr Res , 1999 (presented at

poster session, Am Soc Hum Genet annual meeting, San Francisco, CA, Oct 1999) .


66. Shapiro LR, Gewitz M, Woolf P, Fish B, Ingram S, Golden BF, Marion RW: Recognition of

congenital heart disease as a component of a distinct Prader-Willi syndrome infant

phenotype due to a combination of mosaic trisomy 15 with maternal uniparental

disomy 15. Am J Hum Genet 65:A71,1999 (presented at poster session, Am Soc

Human Genet annual meeting, San Francisco, CA, Oct. 1999).

67. Bogdanow A, Levy P, Shanske AL, Shprintzen RJ, Marion RW: Shprintzen Goldberg

syndrome: Report of 2 affected half siblings. Am J Hum Genet 65:A143, 1999

(presented at poster session, Am Soc Hum Genet annual meeting, San Francisco,

CA, Oct, 1999).

68. Goodrich JT, Orlow S, Staffenberg D, Marion R, Eisig S, Shanske A: Unusual distribution of

acanthosis nigricans in Crouzonodermatoskeletal syndrome. Am J Hum Genet

65:A150, 1999 (presented at poster session, Am Soc Hum Genet annual meeting,

San Francisco, CA, Oct. 1999).

69. Schneider EN, Bogdanow A, Goodrich JT, Marion RW, Cohen MM Jr: Fronto-ocular

dysplasia: A newly recognized trigonocephaly syndrome. Am J Hum Genet

65:A343, 1999 (presented at poster session, Am Soc Hum Genet meeting, SF, CA,

Oct, 1999).

70. Shanske A, Kang H, Shprintzen RJ, Goodrich J, Marion R: Proteus syndrome with infantile

myofibromatosis and severely disturbed adipose growth and differentiation. Am J

Hum Genet 65:A344, 1999 (presented at poster session, Am Soc Hum Genet annual

meeting, San Francisco, CA, 1999).

71. Orlow SJ, Marion R, Duncan C, Gu H, Genovese M, Jenkins E, Shanske A: Hypohidrotic

ectodermal dysplasia and hypomelanosis of Ito in a girl with a de novo

transolocation (X:13)(q13;p11.2). Am J Hum Genet 65:A353, 1999 (presented at

poster session, Am Soc Hum Gen annual meeting, San Fran, CA, Oct, 1999).

72. Shanske AL, Korkko J, Marion R: The "Marshall Chronicles:" Splicing mutation of 54-bp

exon in the COL11A1 gene not found in four generation family with Marshall

syndrome (MIM 154780). Am J Hum Genet 67:110; 2000 (presented at poster

session, Am Soc Human Genetics annual meeting, Philadelphia, Oct, 2000).

73. Marion RW, Mendelson A: First, the bad news: What people with Marfan syndrome (MS)

find when they search the internet for information. Am J Hum Genet 67:203, 2000

(presented at poster session, Am Soc Human Genetics annual meeting, Philadelphia,

October, 2000).


74. Carter S, Einy R, Bobby P, Marion R: Hypermobility type (HT) Ehlers Danlos syndrome

(EDS) and pregnancy: A Case Report. Am J Hum Genet 67:414, 2000 (presented at

poster session, Am Soc Human Genetics annual meeting, Philadelphia, Oct, 2000).

75. Gogineni SK, Wieting I, Shanske A, Marion RW, Iacoboni D, Gross SJ, Nitowsky HM, Carter

SM, Ehrnepreis R, Goldberg Y, Bobby P, Pulijaal VR: Molecular cytogenetic

studies in a family with a half cryptic translocation involving the Wolf-

Hirschorn syndrome critical region. Am J. Hum Genet 69:317, 2001 (presented at

poster session, Am Soc Human Genetics annual meeting, San Diego, CA, Oct 15,

2001).

76. Pulijaal VR, Gogineni SK, Gross SJ, Iacoboni D, Marion RW, Shanske A: Molecular

characterization of a satellited chromosome 22 in a patient with mental retardation

and no dysmorphic features. Am J Hum Genet 69:327, 2001 (presented at poster

session, Am Soc Human Genetics annual meeting, San Diego, October 16, 2001).

77. Eckstein O, Marion R, Upadhayama M, Xin W, Stemmer-Rachamimov A, MacCollin M:

Familial occurrence of both neurofibromatosis 1 and neurofibromatosis 2: Clinical

and molecular analysis (presented at poster session, Annual Clinical Genetics

meetings, New Orleans, LA, March 2002).

78. Dolan SM, Bracero P, Riess A, Shanske AL, Marion RW, Gross S: First trimester diagnosis

of Bartsocas-Papas syndrome by transvaginal sonography: Case report and review of

the literature. (presented at poster session, Annual Clinical Genetics meetings, New

Orleans, LA, March 2002).

79. Marion RW, Schendel L, Hantman E: Folic acid fortification decreases the rate of spina bifida

(SB) in an inner city population by 67%. Am J Hum Genet 71: 366a, 2002

(presented at poster session at the American Soc Human Genet meeting,

Baltimore, MD, October 2002).

80. Shur N, Vega-Rich C, Shanske AL, Marion RW: Non-lethal form of rhizomelic

chondrodysplasia punctata: Report of a case and review of the literature. Am J Hum

Genet 71: 413a, 2002. (presented at poster session at the Am Soc Human Genetics

meetings, Baltimore, MD, October 2002).

81. Goodrich JT, Harmatz P, Levy PA, Marion RW: Loss of vision in MPS VI is a consequence

of increased intracranial pressure. Am J Hum Genet 71:423a, 2002 (presented at

poster session, Am Soc of Human Genetics meeting, Baltimore, MD, October 2002).

82. Marion R, Campbell C: Teaching genomic medicine to third year medical students: The

Einstein experience. Am J Human Genet 73:361, 2003 (presented at a poster

session, Am Soc Human Genetics meeting, Los Angeles, November 2003).


83. Shur N, Marion R et al. Rhizomelic chondrodysplasia punctata and maternal autoimmune

disease: A new case and review of the literature. Am J Human Genet 73:263, 2003

(presented at a poster session, Am Soc Human Genetics meeting, Los Angeles,

November 2003).

84. Barbouth D, Zohouri M, Ramesh KH, Cannizzaro LA, Pulijaal VR, Marion RW: Atypical

phenotype associated with del 18q21.31: Case study and review of the literature.

Am J Hum Genet 73:277, 2003 (presented at poster session, Am Soc Hum

Genetics meeting, Los Angeles, November 2003)

85. Levy PA, Marion RW: Teaching about genetic disorders: A survey of resident understanding

of inborn errors of metabolism. Am J Hum Genet 73:361, 2003 (presented at a

poster session, Am Soc Human Genetics meeting, Los Angeles, November 2003).

86. Miller S, Marion RW et al: Workshop: Teaching Genomic Medicine to Pediatric Clerks: The

Future is now! (presented at Pediatric Academic Society meetings, San Francisco,

CA, May 4, 2004).

87. Marion R, Goodrich J, Staffenberg D: Staged separation of craniopagus conjoined twins:

Medical and neurodevelopmental follow-up one year after separation. Abstract Book, p 140

(presented at a poster session, Am Soc Human Genetics 55th

Annual Meeting, Salt Lake

City, Utah, Oct 25-29, 2005).

88. Shur N, Dolan S, Klugman S, Gross S, Marion R: The potential for false reassurance in

prenatal care: The case of a 37 year old woman with a normal quad screen and a baby born

with Down syndrome (presented at platform session, Am College of Medical Genetics

meeting, San Diego, CA, March 24, 2006).

89. Marion R, Shur N, Peeters N, Wuyts W: A novel pathologic variant in the WFS1 gene in a

patient with Wolfram syndrome (presented at poster session, Am College of Med Genetics

meeting, San Diego, CA, March 25, 2006).

90. Samanich J, Shur N, Marion R: The “Genetic Picture of the Week” Contest: An interactive

method for teaching syndromes to residents (presented at poster session, PAS meetings, San

Francisco, CA, May 1, 2006).

91. Shur N, Marion R, Samanich J, Schaffer J, Roe A: An atypical presentation of systemic

epidermal nevus syndrome in childhood. Abstract book (presented at poster session, Am Soc

Human Genetics 56th

Annual Meeting, New Orleans, LA, Oct 10, 2006)


92. Shur N, Marion R: The Geneticist’s view of Legg-Calvé-Perthes Disease: A Case Report that

Suggests the Need to Screen for Inherited Thrombophilias. Presented at poster session,

American College of Medical Genetics meeting, Florida, February 2007.

93. Samanich J, Fiorino E, Vicencio A, Marion R: A Southern Italian CFTR mutation in a

Jordanian girl with cystic fibrosis (CF). Presented at poster session, American College of

Medical Genetics annual meeting, Florida, February 2007.

94. Marion R, Schendel, L, Goodrich J, Seimon L, Kogan S, Borkow R: The Spina Bifida Clinic

at Blythedale: A 20 year perspective. (presented at poster presentation, Am Soc Human

Genetics 57th

Annual Meeting, San Diego, CA, Oct, 2007).

95. Shur N, Marion R, Greally J: An unusual finding in a child with a presumably balanced

11:22 translocation: The importance of array CGH. (presented at poster session, Am Soc

Human Genetics 57th

Annual Meeting, San Diego, CA, Oct, 2007).

96. Marion RW: The Spina Bifida Clinic at Blythedale: A 20 year perspective. (presented at

Platform session, AUCD annual meeting, Washington DC, Nov 2007).

97. Valicenti-McDermott M, Burrows B, Tibbetts J, Marion R, Shulman L: Advancing maternal

age in children with an Autism Spectrum Disorder and Language Regression (presented at

poster session, PAS annual meeting, Honolulu, Hawaii, May 2008).

98. Pope KO, Paljevic ED, Walsh CA, McDonald T, Marion RW: Caring for families at risk for

sudden death (SD): The organization and early outcomes of a multidisciplinary cardiogenetics

clinic (presented at poster session, American Society of Human Genetics 58th

Annual

Meeting, November 2008, Philadelphia, PA).

99. Babcock M, Samanich J, Marion RW, Levy P, Shanske A, Pope K, Yachelevich N, Hsu DT,

Pan Q, Huang KT, Cannizzaro L, Ramesh KH, Montagna C, Flynn L, Morrow BE: Copy

number variations associated with developmental disorders in a Bronx minority population

(presented at poster session, American Soc Human Genetics 59th

annual meeting,

Honolulu, Hawaii, Oct 21, 2009.

100. Cole PD, Dorfman A, Marion RW, O’Hanlon-Curry J: Methotrexate induces measurable

deficits in verbal memory within days of exposure. Am Soc of Pediatr Hem/Onc

(submitted for presentation).

101. Marion R, Valicenti-McDermott R,M, Grider T, Burrows B: Maternal age distribution at

the time of birth of children with autism spectrum disorder (presented at poster

symposium, PAS Annual Meeting, Vancouver BC, Canada, May 2010).


102. Ridgway E, Kornhaber L, Siegel, J, Cantres L, Marion R: Enabling community

participation for adults with spina bifida in the Bronx (presented at poster session,

ASB, April 2010)

103. Tan B-H, Song C, Tester DJ, Zhou Q, Marion RW, McDonald TV, Ackerman MJ,

Makielski JC: Arrhythmogenic biophysical phenotype for SCN5A mutation S1787N

depends upon splice variant background and low pH. American Heart Association 2010

annual meeting (submitted).

104. Dolan SM, Marion RW, McDonald TV, Wasserman D: Ethical and social implication of

genetic testing in the case of unexpected deaths: Translational of cardiogenic knowledge to

clinical practice. International Conference on Perinatal and Infant Death Annual Meeting

(selected for platform presentation).

105. DeGroat N, Cohen L, Marion RW, Walsh CA, McDonald TV, Dolan SM: Ethical, legal,

and social implications of genetic testing in the case of unexpected deaths: The translation

of cardiogenetic knowledge to clinical practice. 4th

National Conference on Genomics and

Public Health: Using Genomic Information to Improve Health Now and in the Future

(submitted).

106. McDermott DA, Cohen LL, Dolan SM, Marion R: Cardiogenetics: Developing a Model for

Successful Implementation of Personalized Genetic Medicine. (presented at poster session,

ASHG annual meeting, Washington DC, November 2010)

D. Letters to the editor

1. Marion RW, Wiznia AA, Hutcheon RG, Rubinstein A: HIV embryopathy and

neurocristopathies (response to letter by Calvani). Am J Dis Child 142: 10; 1988.

2. Marion RW: Reply to letter re: "A Dip in the Pool." JAMA 259:1496; 1988.

3. Marion RW, Wiznia AA, Hutcheon RG, Rubinstein A: Craniofacial dysmorphism in children

with human immunodeficiency virus infection [Letter]. J Pediatr 113:784; 1988.

4. Marion RW: Eleven pairs of ribs in trisomy 18 [Response to a letter by Ho]. J Pediatr

114:902,1989.

5. Karasik JB, Marion RW: Gastrointestinal and renal malformations associated with prenatal

exposure to alcohol and other teratogens. Am J Med Genet 42:853, 1992.

6. Marion RW: Response to Dr. Hook re. "The Unsolvable Puzzle." Am J Med Genet


7. Shanske A, Bogdanow A, Shprintzen RJ, Marion RW: Marshall syndrome and a defect at the

COL11A1 locus. Am J Med Genet 63:1558-61, 1998

8. Shanske AL, Marion RW: Mosaic trisomy of a small r(1) with an abnormal phenotype. Am J

Med Genet 110:413, 2002

(last updated: 04/23/10)

curriculum vitae - biomedical research · curriculum vitae 1. name: robert w. marion, m.d. offices...

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