Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3
一项全基因组关联研究旨在寻找22q11.2缺失综合征中法洛四联症的修饰基因，该研究在5q14.3上的GPR98基因座中发现了变异。
期刊:Circulation-Cardiovascular Genetics
影响因子:
doi:10.1161/CIRCGENETICS.116.001690
Guo, Tingwei; Repetto, Gabriela M; McDonald McGinn, Donna M; Chung, Jonathan H; Nomaru, Hiroko; Campbell, Christopher L; Blonska, Anna; Bassett, Anne S; Chow, Eva W C; Mlynarski, Elisabeth E; Swillen, Ann; Vermeesch, Joris; Devriendt, Koen; Gothelf, Doron; Carmel, Miri; Michaelovsky, Elena; Schneider, Maude; Eliez, Stephan; Antonarakis, Stylianos E; Coleman, Karlene; Tomita-Mitchell, Aoy; Mitchell, Michael E; Digilio, M Cristina; Dallapiccola, Bruno; Marino, Bruno; Philip, Nicole; Busa, Tiffany; Kushan-Wells, Leila; Bearden, Carrie E; Piotrowicz, Małgorzata; Hawuła, Wanda; Roberts, Amy E; Tassone, Flora; Simon, Tony J; van Duin, Esther D A; van Amelsvoort, Thérèse A; Kates, Wendy R; Zackai, Elaine; Johnston, H Richard; Cutler, David J; Agopian, A J; Goldmuntz, Elizabeth; Mitchell, Laura E; Wang, Tao; Emanuel, Beverly S; Morrow, Bernice E
