A carregar...
Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia
The KE family is a large three‐generational pedigree in which half of the members suffer from a verbal and orofacial dyspraxia in association with a point mutation in the FOXP2 gene. This report extends previous voxel‐based morphometric analyses of magnetic resonance imaging (MRI) scans (Watkins et...
Na minha lista:
| Publicado no: | Hum Brain Mapp |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley Subscription Services, Inc., A Wiley Company
2003
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6872113/ https://ncbi.nlm.nih.gov/pubmed/12599277 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hbm.10093 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|