论文信息 - 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 - 字舞流文

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

Robert W. Mills | A J Agopian | Jonathan H. Chung | K. Lunetta | E. Zackai | K. Coleman | L. Mirny | E. Benjamin | P. Ellinor | D. Cutler | T. van Amelsvoort | S. Antonarakis | B. Morrow | K. Devriendt | J. Vermeesch | C. Bearden | Maxim Imakaev | S. Eliez | A. Bassett | M. Digilio | G. Vlahakes | N. Philip | G. Repetto | B. Emanuel | B. Dallapiccola | S. Lubitz | W. Kates | E. Goldmuntz | A. Roberts | B. Marino | E. Chow | F. Tassone | Christopher L. Campbell | L. E. Mitchell | D. Milan | N. Tucker | Victoria A. Parsons | Moritz F. Sinner | L. Weng | T. Simon | M. Mitchell | E. Dolmatova | E. Mlynarski | A. Swillen | Maude Schneider | A. Tomita-Mitchell | W. Hucker | H. Jameson | H. Johnston | T. Guo | D. Gothelf | J. Leyton-Mange | A. Blonska | T. Busa | E. V. van Duin | Donna M. McDonald McGinn | H. Nomaru | M. Carmel | E. Michaelovsky | Leila Kushan-Wells | M. Piotrowicz | Wanda Hawuła | Tao Wang | Jiangchuan Ye | Rebecca R. Cooper | Honghuang Lin