Social Cognition in Williams Syndrome: Genotype/Phenotype Insights from Partial Deletion Patients

Identifying genotype/phenotype relations in human social cognition has been enhanced by the study of Williams syndrome (WS). Indeed, individuals with WS present with a particularly strong social drive, and researchers have sought to link deleted genes in the WS critical region (WSCR) of chromosome 7...

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Detalles Bibliográficos
Autores principales: Karmiloff-Smith, Annette, Broadbent, Hannah, Farran, Emily K., Longhi, Elena, D’Souza, Dean, Metcalfe, Kay, Tassabehji, May, Wu, Rachel, Senju, Atsushi, Happé, Francesca, Turnpenny, Peter, Sansbury, Francis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Psychology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362742/
https://www.ncbi.nlm.nih.gov/pubmed/22661963
http://dx.doi.org/10.3389/fpsyg.2012.00168

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3362742/
https://www.ncbi.nlm.nih.gov/pubmed/22661963
http://dx.doi.org/10.3389/fpsyg.2012.00168

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