Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16
针对多种先天性心脏病表型的全基因组关联研究，在4p16染色体上发现了一个房间隔缺损的易感基因位点
期刊:Nature Genetics
影响因子:29
doi:10.1038/ng.2637
Cordell, Heather J; Bentham, Jamie; Topf, Ana; Zelenika, Diana; Heath, Simon; Mamasoula, Chrysovalanto; Cosgrove, Catherine; Blue, Gillian; Granados-Riveron, Javier; Setchfield, Kerry; Thornborough, Chris; Breckpot, Jeroen; Soemedi, Rachel; Martin, Ruairidh; Rahman, Thahira J; Hall, Darroch; van Engelen, Klaartje; Moorman, Antoon F M; Zwinderman, Aelko H; Barnett, Phil; Koopmann, Tamara T; Adriaens, Michiel E; Varro, Andras; George, Alfred L Jr; dos Remedios, Christobal; Bishopric, Nanette H; Bezzina, Connie R; O'Sullivan, John; Gewillig, Marc; Bu'Lock, Frances A; Winlaw, David; Bhattacharya, Shoumo; Devriendt, Koen; Brook, J David; Mulder, Barbara J M; Mital, Seema; Postma, Alex V; Lathrop, G Mark; Farrall, Martin; Goodship, Judith A; Keavney, Bernard D
