A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome.

Urreizti, Roser; Damanti, Sarah; Esteve, Carla; Franco-Valls, Héctor; Castilla-Vallmanya, Laura; Tonda, Raul; Cormand, Bru; Vilageliu, Lluïsa; Opitz, John M; Neri, Giovanni; Grinberg, Daniel; Balcells, Susana.
Sci Rep; 8(1): 694, 2018 01 12.
Artigo em Inglês | MEDLINE | ID: mdl-29330474