Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects

Author:

Zhao Yingjie,Diacou Alexander,Johnston H. Richard,Musfee Fadi I.,McDonald-McGinn Donna M.,McGinn Daniel,Crowley T. Blaine,Repetto Gabriela M.,Swillen Ann,Breckpot Jeroen,Vermeesch Joris R.,Kates Wendy R.,Digilio M. Cristina,Unolt Marta,Marino Bruno,Pontillo Maria,Armando Marco,Di Fabio Fabio,Vicari Stefano,van den Bree Marianne,Moss Hayley,Owen Michael J.,Murphy Kieran C.,Murphy Clodagh M.,Murphy Declan,Schoch Kelly,Shashi Vandana,Tassone Flora,Simon Tony J.,Shprintzen Robert J.,Campbell Linda,Philip Nicole,Heine-Suñer Damian,García-Miñaúr Sixto,Fernández Luis,Bearden Carrie E.,Vingerhoets Claudia,van Amelsvoort Therese,Eliez Stephan,Schneider Maude,Vorstman Jacob A.S.,Gothelf Doron,Zackai Elaine,Agopian A.J.,Gur Raquel E.,Bassett Anne S.,Emanuel Beverly S.,Goldmuntz Elizabeth,Mitchell Laura E.,Wang Tao,Morrow Bernice E.,Antonarakis Stylianos E.,Biondi Massimo,Boot Erik,Breetvelt Elemi,Busa Tiffany,Butcher Nancy,Buzzanca Antonino,Carmel Miri,Cleynen Isabelle,Cutler David,Dallapiccola Bruno,de la Fuente Sanches María Angeles,Epstein Michael P.,Evers Rens,Fernandez Luis,Fritsch Rosemarie,Algas Fernando García,Guo Tingwei,Gur Raquel,Hestand Matthew S.,Heung Tracy,Hooper Stephen,Jin Andrea,Kushan-Wells Leila,Laorden-Nieto Alejandra Teresa,Lattanzi Guido,Marshall Christian,McCabe Kathryn,Michaelovsky Elena,Ornstein Claudia,Silversides Candice,Tran Oanh,van Duin Esther D.A.,Vergaelen Elfi,Warren Steve T.,Weinberger Ronnie,Weizman Abraham,Zhang Zhengdong,Zwick Michael

Funder

National Institutes of Health

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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