Rapid one-day fluorescence in situ hybridisation in prenatal diagnosis using uncultured amniocytes and chorionic villi

Annals of the Academy of Medicine Singapore

Volumn 28, Issue 4, 1999, Pages 502-507

  Cai, L S ^b   Lim, A S T ^b   Tan, Ann ^a  

^a SINGAPORE GENERAL HOSPITAL   (Singapore)

^b NONE

Author keywords

Karyotyping; Maternal cell contamination; Mosaicism; Trisomy

Indexed keywords

ADULT; AMNION; ANEUPLOIDY; ARTICLE; CHORION VILLUS SAMPLING; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME ABERRATION; CHROMOSOME DISORDER; CYTOLOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HIGH RISK PREGNANCY; HUMAN; MATERNAL AGE; METHODOLOGY; PREGNANCY; PRENATAL DIAGNOSIS; SEX CHROMOSOME ABERRATION; TIME; X CHROMOSOME; Y CHROMOSOME;

ADULT; AMNION; ANEUPLOIDY; CHORIONIC VILLI SAMPLING; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 18; CHROMOSOMES, HUMAN, PAIR 21; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MATERNAL AGE; PREGNANCY; PREGNANCY, HIGH-RISK; PRENATAL DIAGNOSIS; SEX CHROMOSOME ABERRATIONS; TIME FACTORS; X CHROMOSOME; Y CHROMOSOME;

EID: 0033161905     PISSN: 03044602     EISSN: 29724066     Source Type: Journal    
DOI: None     Document Type: Article

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