Absence of SYCP3 mutations in women with recurrent miscarriage with at least one trisomic miscarriage

Reproductive BioMedicine Online

Volumn 24, Issue 2, 2012, Pages 251-253

  Hanna, Courtney W ^a   Blair, John D ^a   Stephenson, Mary D ^a,b   Robinson, Wendy P ^a  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b UNIVERSITY OF CHICAGO   (United States)

Author keywords

mutations; nondisjunction; recurrent miscarriage; SYCP3; trisomy

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; EXON; FEMALE; GENE; GENE MUTATION; HUMAN; INTRON; JAPANESE; MEIOSIS; RECURRENCE RISK; RECURRENT ABORTION; SPONTANEOUS ABORTION; SYCP3 GENE; TRISOMY;

ABORTION, HABITUAL; ADULT; CHROMOSOMES, HUMAN, 13-15; CHROMOSOMES, HUMAN, 21-22 AND Y; CHROMOSOMES, HUMAN, PAIR 16; FEMALE; HUMANS; MOSAICISM; NONDISJUNCTION, GENETIC; NUCLEAR PROTEINS; SYNAPTONEMAL COMPLEX; TRISOMY;

EID: 84856653640     PISSN: 14726483     EISSN: 14726491     Source Type: Journal    
DOI: 10.1016/j.rbmo.2011.10.013     Document Type: Article

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