Case report: Chromatid exchange and predivision of chromatids as other sources of abnormal oocytes detected by preimplantation genetic diagnosis of translocations

Prenatal Diagnosis

Volumn 18, Issue 13, 1998, Pages 1450-1458

  Munné, Santiago ^a   Bahçe, Muhterem ^b   Schimmel, Tim ^a   Sadowy, Sasha ^a   Cohen, Jacques ^a  

^a SAINT BARNABAS MEDICAL CENTER   (United States)

^b GULHANE SCHOOL OF MEDICINE   (Turkey)

Author keywords

Preimplantation genetic diagnosis; Recombination; Spontaneous abortions; t(11; 16)

Indexed keywords

ADULT; ARTICLE; BLASTOMERE; CASE REPORT; CHROMATID; CHROMATID EXCHANGE; CHROMOSOME 11; CHROMOSOME 16; CHROMOSOME PAINTING; DNA PROBE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE TRANSLOCATION; HUMAN; MEIOSIS; METAPHASE; OOCYTE; PREIMPLANTATION EMBRYO; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

ABORTION, SPONTANEOUS; ADULT; CHROMATIDS; CHROMOSOME PAINTING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 16; EMBRYONIC DEVELOPMENT; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MEIOSIS; METAPHASE; OOCYTES; PREGNANCY; PRENATAL DIAGNOSIS; STAINING AND LABELING; TRANSLOCATION, GENETIC;

EID: 0032415848     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199812)18:13<1450::AID-PD509>3.0.CO;2-Q     Document Type: Article

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