Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome
32 auth. E. Mlynarski, Michael Xie, Deanne M. Taylor, M. Sheridan, T. Guo, S. Racedo, D. McDonald-McGinn, E. Chow, J. Vorstman, A. Swillen, K. Devriendt, J. Breckpot, M. Digilio, B. Marino, B. Dallapiccola, ... N. Philip, T. Simon, A. Roberts, M. Piotrowicz, C. Bearden, S. Eliez, D. Gothelf, K. Coleman, W. Kates, M. Devoto, E. Zackai, D. Heine- Suñer, E. Goldmuntz, A. Bassett, B. Morrow, B. Emanuel, The International HapMap Consortium