Risultati ricerca 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

pubblicato su: CIRCULATION, CARDIOVASCULAR GENETICS - 2017

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 Ma?gorzata, Hawu?a 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.