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Title: | A de novo FOXP1 truncating mutation in a patient originally diagnosed as C Syndrome |
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Author: | Urreizti Frexedas, Roser; Damanti, Sarah; Esteve, Carla; Franco Valls, Héctor; Castilla Vallmanya, Laura; Tonda, Raul; Cormand Rifà, Bru; Vilageliu i Arqués, Lluïsa; Opitz, John M.; Neri, Giovanni; Grinberg Vaisman, Daniel Raúl; Balcells Comas, Susana |
Other authors: | Universitat de Barcelona |
Abstract: | |
Subject(s): | -Mutació (Biologia) -Anomalies cromosòmiques -Mutation (Biology) -Chromosome abnormalities |
Rights: | cc-by (c) Urreizti Frexedas, Roser et al., 2018
http://creativecommons.org/licenses/by/3.0/es |
Document type: | Article Article - Published version |
Published by: | Nature Publishing Group |
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