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Defining the Social Phenotype in Williams Syndrome: A Model for Linking Gene, the Brain, and Behavior

Research into phenotype-genotype correlations in neurodevelopmental disorders has greatly elucidated the contribution of genetic and neurobiological factors to variations in typical and atypical development. Etiologically relatively homogeneous disorders, such as Williams syndrome (WS), provide uniq...

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Detalhes bibliográficos
Main Authors: Järvinen-Pasley, Anna, Bellugi, Ursula, Reilly, Judy, Mills, Debra L., Galaburda, Albert, Reiss, Allan L., Korenberg, Julie R.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2892602/
https://ncbi.nlm.nih.gov/pubmed/18211726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S0954579408000011
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