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...

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Príomhchruthaitheoirí: Belton, E, Salmond, C, Watkins, K, Vargha-Khadem, F, Gadian, D
Formáid: Journal article
Teanga:English
Foilsithe / Cruthaithe: 2003