Prenatal diagnosis of 46,XY/46,XX mosaicism: A case report

American Journal of Medical Genetics

Volumn 84, Issue 1, 1999, Pages 12-14

  Yaron, Yuval ^a   Feldman, Baruch ^a   Kramer, Ralph L ^a   Kasperski, Stefanie B ^a   Vo, Trieu ^a   Feldman, Gerald L ^a   Johnson, Mark P ^a   Evans, Mark I ^a,b   Ebrahim, Salah A D ^a  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WAYNE STATE UNIVERSITY   (United States)

Author keywords

46,XX 46,XY mosaicism; Phenotype; Prenatal diagnosis

Indexed keywords

DNA;

ALLELE; ARTICLE; CASE REPORT; CONTROLLED STUDY; CYTOGENETICS; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MALE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SEX CHROMOSOME MOSAICISM; VARIABLE NUMBER OF TANDEM REPEAT; X CHROMOSOME; Y CHROMOSOME;

ALLELES; APOLIPOPROTEINS B; CHIMERA; FETUS; HUMANS; MALE; MEIOSIS; MINISATELLITE REPEATS; MITOSIS; MOSAICISM; PHENOTYPE; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; SEX CHARACTERISTICS; SEX CHROMOSOMES;

EID: 0033531961     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990507)84:1<12::AID-AJMG3>3.0.CO;2-U     Document Type: Article

References (1)

1. Freiberg AS, Blumberg B, Lawce H, Mann J. 1988. XX/XY chimerism encountered during prenatal diagnosis. Prenat Diagn 8:423-426.