Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells

Human Molecular Genetics

Volumn 1, Issue 5, 1992, Pages 307-313

  Ried, Thomas ^a   Landes, Greg ^a,b   Dackowski, William ^a,b   Klinger, Katherine ^a,b   Ward, David C ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b Integrated Genetics   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMNION FLUID; ANEUPLOIDY; ARTICLE; CHROMOSOME 13; CHROMOSOME 18; COMPUTER PROGRAM; CYTOLOGY; DNA PROBE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC PROCEDURES; HUMAN; MALE; METHODOLOGY; PREGNANCY; PRENATAL DIAGNOSIS; X CHROMOSOME; Y CHROMOSOME;

AMNIOTIC FLUID; ANEUPLOIDY; CHROMOSOMES, HUMAN, PAIR 13; CHROMOSOMES, HUMAN, PAIR 18; DNA PROBES; EVALUATION STUDIES; FEMALE; HUMAN; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MOLECULAR PROBE TECHNIQUES; PREGNANCY; PRENATAL DIAGNOSIS; SOFTWARE; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; X CHROMOSOME; Y CHROMOSOME;

EID: 0026907046     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/1.5.307     Document Type: Article

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