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23. Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome? Baptista MJ; Fairbrother UL; Howard CM; Farrer MJ; Davies GE; Trikka D; Maratou K; Redington A; Greve G; Njølstad PR; Kessling AM Hum Genet; 2000 Nov; 107(5):476-82. PubMed ID: 11140945 [TBL] [Abstract][Full Text] [Related]
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40. De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects. Priest JR; Osoegawa K; Mohammed N; Nanda V; Kundu R; Schultz K; Lammer EJ; Girirajan S; Scheetz T; Waggott D; Haddad F; Reddy S; Bernstein D; Burns T; Steimle JD; Yang XH; Moskowitz IP; Hurles M; Lifton RP; Nickerson D; Bamshad M; Eichler EE; Mital S; Sheffield V; Quertermous T; Gelb BD; Portman M; Ashley EA PLoS Genet; 2016 Apr; 12(4):e1005963. PubMed ID: 27058611 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]