Congenial heart disease revealing familial Velocardiofacial syndrome caused by 3 Mb deletion at 22q11 region - Ribeiro-Bicudo, L. A.; Oliveira, C. C.; Gomes, T. G. [UNESP]; Santos, M. V.; Bergamo, N. A.; Rocha, R. H.; Gamba, B. F. (Nature Publishing Group, 2018)