Is cytogenetic diagnosis of 46,XX karyotype spontaneous abortion specimens erroneous? Fluorescence in situ hybridization as a confirmatory technique

Journal of Obstetrics and Gynaecology Research

Volumn 31, Issue 6, 2005, Pages 508-513

  Karaoguz, Meral Yirmibes ^a   Nas, Tuncay ^a   Konaç, Ece ^a   Ince, Didem ^a   Pala, Elif ^a   Menevse, Sevda ^a  

^a GAZI UNIVERSITY FACULTY OF MEDICINE   (Turkey)

Author keywords

Chromosome anomalies; Fluorescence in situ hybridization technique; Spontaneous abortion; Y chromosome components

Indexed keywords

ADULT; ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME STRUCTURE; CONTROLLED STUDY; CYTOGENETICS; DIAGNOSTIC ACCURACY; DIAGNOSTIC ERROR; DIAGNOSTIC VALUE; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; GESTATIONAL AGE; HUMAN; HUMAN TISSUE; KARYOTYPE 46,XX; KARYOTYPING; MONOSOMY X; SPONTANEOUS ABORTION; TECHNIQUE; TETRAPLOIDY; TISSUE CULTURE; TRISOMY; TRISOMY 15; TRISOMY 16; TRISOMY 21; Y CHROMOSOME;

ABORTION, SPONTANEOUS; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, X; CHROMOSOMES, HUMAN, Y; CYTOGENETIC ANALYSIS; DIAGNOSTIC ERRORS; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MALE; PREGNANCY;

EID: 30344470178     PISSN: 13418076     EISSN: 14470756     Source Type: Journal    
DOI: 10.1111/j.1447-0756.2005.00330.x     Document Type: Article

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