Jeanne Meck

Georgetown University Hospital, Obstetrics and Gynecology, Washington, District of Columbia

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Papers22 papers

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Patient attitudes toward first trimester screening

Andrea Wray,Helain Landy,Jeanne Meck

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, no. SUP6 (2006): S167-S167

EIBibtex

Patient decisions regarding prenatal aneuploid FISH

Andrea Wray,Helain Landy,Jeanne Meck

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, no. SUP6 (2005): S163-S163

EIBibtex

Constitutional trisomy 8 mosaicism due to meiosis II non-disjunction in a phenotypically normal woman with hematologic abnormalities

Said M Baidas, T-J Chen,Valentin Kolev,Leejun C Wong,Joel Imholte,Naigeng Qin,Jeanne M Meck

AMERICAN JOURNAL OF MEDICAL GENETICS PART A, no. 4 (2004): 383-387

Cited by8WOSBibtex

Meconium staining of placenta may be later than conventionally thought

Sarah Poggi,Nia Leak,Alessandro Ghidini,Jonathon Hodor,Jeanne Meck,Carolyn Salafia

AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, no. SUP6 (2003): S192-S192

Cited by1EIBibtex

CD5-negative, CD10-negative small B-cell leukemia: variant of chronic lymphocytic leukemia or a distinct entity

Salwa S Sheikh,Bhaskar V S Kallakury,Khawla A Al-Kuraya,Jeanne Meck,Dan P Hartmann,Adam Bagg

AMERICAN JOURNAL OF HEMATOLOGY, no. 4 (2002): 306-310

Cited by18WOSBibtex

Detection of Chromosomal Aberrations by a Whole-Genome Microsatellite Screen

Marjorie J. Rosenberg,David Vaske,Christina E. Killoran,Yi Ning,David Wargowski,Louanne Hudgins,Cynthia J. Tifft,Jeanne Meck,Jan K. Blancato,Kenneth Rosenbaum,Richard M. Pauli,James Weber

AMERICAN JOURNAL OF HUMAN GENETICS, no. 2 (2000): 419-427

Cited by48EIWOSBibtex

GLI3 deletions associated with Greig cephalopolysyndactyly and implications for phenotypic overlap with Acrocallosal syndrome

IM Olivos-Glander,J Blancato,J Meck,LG Biesecker

AMERICAN JOURNAL OF HUMAN GENETICS, no. SUP4 (2000): 14-14

Bibtex

Molecular analysis of Greig cephalopolysyndactyly syndrome shows a high frequency of deletions

IM Olivos-Glander,J Blancato,J Meck,LG Biesecker

AMERICAN JOURNAL OF HUMAN GENETICS, no. SUP4 (1999): A483-A483

Bibtex

Cytogenetic and molecular evidence of constitutional mosaic trisomy 8 and hematologic abnormalities in a phenotypically normal woman

J Meck, TJ Chen, LJ Wong, J IMholte, K Perry, N Qin, S Baidas

AMERICAN JOURNAL OF HUMAN GENETICS, no. SUP4 (1999): A138-A138

Bibtex

Identification of de novo chromosomal markers and derivatives by spectral karyotyping

B. R. Haddad,Evelin Schröck,Jeanne Meck,Janet Cowan,Hannah Young,Malcolm A. Ferguson-Smith,Stanislas du Manoir,Thomas Ried

Human Genetics, no. 5 (1998): 619-625

Cited by49WOSBibtex

Brief report: association of sex chromosome anomalies with childhood-onset psychotic disorders

S Kumra,E Wiggs,D Krasnewich,J Meck, A C Smith,J Bedwell,T Fernandez,L K Jacobsen,M Lenane,J L Rapoport

Journal of the American Academy of Child and Adolescent Psychiatry, no. 3 (1998): 292-296

Cited by41WOSEIBibtex

Characterization of a supernumerary marker derived from chromosome 17 by microdissection in an adult with MR/MCA

C Kozma,J Blancato,J Meck,Y Jiang

AMERICAN JOURNAL OF MEDICAL GENETICS, no. 1 (1998): 19-22

Cited by11WOSBibtex

Application of spectral karyotyping in clinical cytogenetics

BR Haddad,J Meck,H Young,J Cowan, S duManoir,E Schrock,T Ried

AMERICAN JOURNAL OF HUMAN GENETICS, no. SUP4 (1997): A127-A127

Bibtex

An association between sex chromosome anomalies and childhood psychosis

S Kumra,E Wiggs, LK Jacobsen,D Krasnewich, ACM Smith,J Meck,J Bedwell,M Lenane,JL Rapoport

AMERICAN JOURNAL OF HUMAN GENETICS, no. SUP4 (1997): A131-A131

Bibtex

Combining spectral karyotyping and subtelomeric probes to improve cytogenetic diagnosis

Y Ning, B Huang,J Meck,E Schrock,T Ried

AMERICAN JOURNAL OF HUMAN GENETICS, no. SUP4 (1997): A136-A136

Bibtex

PRENATAL DETECTION OFDE NOVO INVERSION OF CHROMOSOME (2) (p13q11.2) AND POSTNATAL FOLLOW-UP

CHAHIRA KOZMA,CHERYL SUBASINGHE,JEANNE MECK

Prenatal Diagnosis, no. 4 (1996): 366-370

Cited by1Bibtex

Prenatal detection of de novo inversion of chromosome (2) (p13q11.2) and postnatal follow-up

C Kozma,C Subasinghe,J Meck

Prenatal diagnosis, no. 4 (1996): 366-370

Cited by1WOSBibtex

Atypical cholinesterase in a patient with situs inversus totalis

R Nayak,J Meck,M Hannallah

ANESTHESIOLOGY, no. 4 (1995): 881-881

Cited by3WOSBibtex

Prenatal diagnosis of tetrasomy 12p byin situ hybridization: Varying levels of mosaicism in different fetal tissues

J. K. Blancato,M. Hunt,J. George,J. Katz,J. M. Meck

Prenatal Diagnosis, no. 12 (1992): 979-983

Cited by12Bibtex

VARYING LEVELS OF MOSAICISM IN TISSUES OF A PRENATALLY DIAGNOSED CASE OF TETRASOMY 12-P

J BLANCATO, M HUNT, J GEORGE, J KATZ,J MECK

AMERICAN JOURNAL OF HUMAN GENETICS, no. SUP4 (1991): 257-257

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