Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

Elisabeth E. Mlynarski; Michael Xie; Deanne Taylor; Molly B. Sheridan; Tingwei Guo; Silvia E. Racedo; Donna M. McDonald-McGinn; Eva W. C. Chow; Jacob Vorstman; Ann Swillen; Koen Devriendt; Jeroen Breckpot; Maria Cristina Digilio; Bruno Marino; Bruno Dallapiccola; Nicole Philip; Tony J. Simon; Amy E. Roberts; Małgorzata Piotrowicz; Carrie E. Bearden; Stephan Eliez; Doron Gothelf; Karlene Coleman; Wendy R. Kates; Marcella Devoto; Elaine Zackai; Damian Heine- Suñer; Elizabeth Goldmuntz; Anne S. Bassett; Bernice E. Morrow; Beverly S. Emanuel