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A Genetic Model for Understanding Higher Order Visual Processing: Functional Interactions of the Ventral Visual Stream in Williams Syndrome

Williams syndrome (WS) is a rare neurodevelopmental disorder caused by a 1.6 Mb microdeletion on chromosome 7q11.23 and characterized by hypersocial personality and prominent visuospatial construction impairments. Previous WS studies have identified functional and structural abnormalities in the hip...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Sarpal, Deepak, Buchsbaum, Bradley R., Kohn, Philip D., Kippenhan, J. Shane, Mervis, Carolyn B., Morris, Colleen A., Meyer-Lindenberg, Andreas, Berman, Karen Faith
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2008
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2733313/
https://ncbi.nlm.nih.gov/pubmed/18308711
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cercor/bhn004
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