Deletion size and background genetic variation shape congenital heart disease phenotypes in 3016 individuals with 22q11.2 deletion syndrome.

Lin Jhih-Rong, Miller Daniella, Luong Dana, Nelson Tanner, Crowley T B, Tran Oanh T, Thiruvahindrapuram Bhooma, Hajianpour Amirhossein, Campbell Linda, Busa Tiffany, Heine-Suñer Damian, García-Miñaúr Sixto, Fernández Luis, Murphy Kieran C, Murphy Declan G, Hawula Wanda, Angkustsiri Kathleen, Shashi Vandana, Schoch Kelly, Bearden Carrie E, Tomita-Mitchell Aoy, Mitchell Michael, Carmel Miri, Weizman Abraham, Michaelovsky Elena, Gothelf Doron, van den Bree Marianne, Owen Michael, Vorstman Jacob, Boot Erik, Vingerhoets Claudia, Van Amelsvoort Therese, Swillen Ann, Breckpot Jeroen, R Vermeesch Joris, Devriendt Koenraad, Schneider Maude, Eliez Stephan, Digilio Maria Cristina, Unolt Marta, Putotto Carolina, Versacci Paolo, Marino Bruno, Pontillo Maria, Armando Marco, Vicari Stefano, Repetto Gabriela M, Kates Wendy, Shprintzen Robert J, Gur Raquel E, Zackai Elaine, Goldmuntz Elizabeth, Wang Tao, Raj Srilakshmi, Emanuel Beverly S, McDonald-McGinn Donna M, Scherer Stephen W, Bassett Anne S, Zhang Zhengdong D, Morrow Bernice E

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