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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...

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Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2009
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Accesso online: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
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