Prenatal diagnosis with use of fetal cells isolated from maternal blood: Five-color fluorescent in situ hybridization analysis on flow-sorted cells for chromosomes X, Y, 13, 18, and 21

American Journal of Obstetrics and Gynecology

Volumn 179, Issue 1, 1998, Pages 203-209

  Bischoff, F Z ^a   Lewis, D E ^a   Nguyen, D D ^a   Murrell, S ^a   Schober, W ^a   Scott, J ^a   Simpson, J L ^a   Elias, S ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

Fetal cells in maternal blood; Flow cytometry; Fluorescence in situ hybridization

Indexed keywords

ARTICLE; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME ANALYSIS; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FETUS; FETUS CELL; FLOW CYTOMETRY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MATERNAL BLOOD; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; X CHROMOSOME; Y CHROMOSOME;

EID: 0031857282     PISSN: 00029378     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9378(98)70273-X     Document Type: Article

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