Prenatal diagnosis of 46,XX male fetuses

American Journal of Obstetrics and Gynecology

Volumn 180, Issue 4, 1999, Pages 1006-1007

  Ginsberg, Norman A ^a   Cadkin, Alan ^a   Strom, Charles ^a   Bauer Marsh, Elizabeth ^a   Verlinsky, Yury ^a  

^a NONE

Author keywords

46,XX male; Amniocentesis during second trimester; Intersex; Prenatal; SRY gene; Ultrasonography

Indexed keywords

AMNIOCENTESIS; CASE REPORT; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; CONFERENCE PAPER; FETUS; FETUS ECHOGRAPHY; GENETIC ANALYSIS; HUMAN; KARYOTYPING; MALE; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SEX DIFFERENCE; TESTICULAR FEMINIZATION; X CHROMOSOME; Y CHROMOSOME;

EID: 0032901563     PISSN: 00029378     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9378(99)70673-3     Document Type: Conference Paper

References (2)

1. 1. de la Chapelle A. Analytical review: nature and origin of males with XX sex chromosomes. Am J Hum Genet 1972;24:71-105.
2. 2. Haqq CM, King C-Y, Ukiyama E, Falsafi S, Haaqq TN, Donohoee PK, et al. Molecular basis of mammalian sexual determination: activation of mullerian inhibiting substance gene expression by SRY. Science 1994;266:1494-500.