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收藏Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot
Cordell, Heather J.; Toepf, Ana; Mamasoula, Chrysovalanto; Postma, Alex V.; Bentham, Jamie; Zelenika, Diana; Heath, Simon; Blue, Gillian; Cosgrove, Catherine; Riveron, Javier Granados; Darlay, Rebecca; Soemedi, Rachel; Wilson, Ian J.; Ayers, Kristin L.; Rahman, Thahira J.; Hall, Darroch; Mulder, Barbara J. M.; Zwinderman, Aelko H.; van Engelen, Klaartje; Brook, J. David; Setchfield, Kerry; Bu'Lock, Frances A.; Thornborough, Chris; O'Sullivan, John; Stuart, A. Graham; Parsons, Jonathan; Bhattacharya, Shoumo; Winlaw, David; Mital, Seema; Gewillig, Marc; Breckpot, Jeroen; Devriendt, Koen; Moorman, Antoon F. M.; Rauch, Anita; Lathrop, G. Mark; Keavney, Bernard D.; Goodship, Judith A.
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收藏Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants
Griffin, Helen R.; Toepf, Ana; Glen, Elise; Zweier, Christiane; Stuart, A. Graham; Parsons, Jonathan; Peart, Ian; Deanfield, John; O'Sullivan, John; Rauch, Anita; Scambler, Peter; Burn, John; Cordell, Heather J.; Keavney, Bernard; Goodship, Judith A.
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