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dc.contributor | Universitat de Barcelona |
---|---|
dc.contributor.author | Urreizti Frexedas, Roser |
dc.contributor.author | Damanti, Sarah |
dc.contributor.author | Esteve, Carla |
dc.contributor.author | Franco Valls, Héctor |
dc.contributor.author | Castilla Vallmanya, Laura |
dc.contributor.author | Tonda, Raul |
dc.contributor.author | Cormand Rifà, Bru |
dc.contributor.author | Vilageliu i Arqués, Lluïsa |
dc.contributor.author | Opitz, John M. |
dc.contributor.author | Neri, Giovanni |
dc.contributor.author | Grinberg Vaisman, Daniel Raúl |
dc.contributor.author | Balcells Comas, Susana |
dc.date | 2018-01-23T15:55:35Z |
dc.date | 2018-01-23T15:55:35Z |
dc.date | 2018-01-12 |
dc.date | 2018-01-23T15:55:36Z |
dc.identifier.citation | 2045-2322 |
dc.identifier.citation | 671804 |
dc.identifier.uri | http://hdl.handle.net/2445/119240 |
dc.format | 6 p. |
dc.format | application/pdf |
dc.language.iso | eng |
dc.publisher | Nature Publishing Group |
dc.relation | Reproducció del document publicat a: https://doi.org/10.138/s41598-017-19109-0 |
dc.relation | Scientific Reports, 2018, vol. 8, p. 694-1-694-6 |
dc.relation | https://doi.org/10.138/s41598-017-19109-0 |
dc.rights | cc-by (c) Urreizti Frexedas, Roser et al., 2018 |
dc.rights | info:eu-repo/semantics/openAccess |
dc.rights | http://creativecommons.org/licenses/by/3.0/es |
dc.subject | Mutació (Biologia) |
dc.subject | Anomalies cromosòmiques |
dc.subject | Mutation (Biology) |
dc.subject | Chromosome abnormalities |
dc.title | A de novo FOXP1 truncating mutation in a patient originally diagnosed as C Syndrome |
dc.type | info:eu-repo/semantics/article |
dc.type | info:eu-repo/semantics/publishedVersion |
dc.description.abstract |