A carregar...

Alterations in Midline Cortical Thickness and Gyrification Patterns Mapped in Children with 22q11.2 Deletions

The 22q11.2 deletion syndrome (velocardiofacial/DiGeorge syndrome) is a neurogenetic condition associated with visuospatial deficits, as well as elevated rates of attentional disturbance, mood disorder, and psychosis. Previously, we detected pronounced cortical thinning in superior parietal and righ...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Bearden, Carrie E., van Erp, Theo G.M., Dutton, Rebecca A., Lee, Agatha D., Simon, Tony J., Cannon, Tyrone D., Emanuel, Beverly S., McDonald-McGinn, Donna, Zackai, Elaine H., Thompson, Paul M.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2733329/
https://ncbi.nlm.nih.gov/pubmed/18483006
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/cercor/bhn064
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!