Social Brain Development in Williams Syndrome: The Current Status and Directions for Future Research

Williams syndrome (WS) is a neurodevelopmental condition that occurs as a result of a contiguous deletion of ∼26–28 genes on chromosome 7q11.23. WS is often associated with a distinctive social phenotype characterized by an increased affinity toward processing faces, reduced sensitivity to fear rela...

Descripción completa

Detalles Bibliográficos
Autores principales: Haas, Brian W., Reiss, Allan L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Psychology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3370330/
https://www.ncbi.nlm.nih.gov/pubmed/22701108
http://dx.doi.org/10.3389/fpsyg.2012.00186

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3370330/
https://www.ncbi.nlm.nih.gov/pubmed/22701108
http://dx.doi.org/10.3389/fpsyg.2012.00186

Ejemplares similares