Pubblicazioni

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

2017 - CIRCULATION, CARDIOVASCULAR GENETICS

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, MaÅgorzata; HawuÅa, Wanda; Roberts, Amy E.; Tassone, Flora; Simon, Tony J.; Van Duin, Esther D. A.; Van Amelsvoort, ThÃ©rÃ¨se 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.