Preimplantation diagnosis by fluorescence in situ hybridization using 13-, 16-, 18-, 21-, 22-, X-, and Y-chromosome probes

Journal of Assisted Reproduction and Genetics

Volumn 16, Issue 2, 1999, Pages 92-96

  Sasabe, Yutaka ^a   Katayama, K Paul ^b   Nishimura, Takayo ^a   Takahashi, Akiko ^a   Asakura, Hiroyuki ^b   Winchester Peden, Kristen ^b   Wise, Laura ^b   Abe, Yuji ^a   Kubo, Harumi ^a   Hirakawa, Shun ^a  

^a TOHO UNIVERSITY   (Japan)

^b Advanced Institute of Fertility   (United States)

Author keywords

Chromosomal anomaly; Fluorescence in situ hybridization; Karyotype analysis; Preimplantation diagnosis; Spontaneous abortion

Indexed keywords

ANEUPLOIDY; ARTICLE; BLASTOMERE; CHROMOSOME 13; CHROMOSOME 16; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME 22; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KARYOTYPING; PREIMPLANTATION EMBRYO; PRIORITY JOURNAL; X CHROMOSOME; Y CHROMOSOME;

ABORTION, SPONTANEOUS; ADULT; ANEUPLOIDY; BIOPSY; BLASTOMERES; CHROMOSOMES, HUMAN; DNA PROBES; FEASIBILITY STUDIES; FEMALE; FERTILIZATION IN VITRO; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; PREGNANCY; PREIMPLANTATION DIAGNOSIS; X CHROMOSOME; Y CHROMOSOME;

EID: 0033015785     PISSN: 10580468     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1022520907332     Document Type: Article

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