Atypical cortical connectivity and visuospatial cognitive impairments are related in children with chromosome 22q11.2 deletion syndrome

BACKGROUND: Chromosome 22q11.2 deletion syndrome is one of the most common genetic causes of cognitive impairment and developmental disability yet little is known about the neural bases of those challenges. Here we expand upon our previous neurocognitive studies by specifically investigating the hyp...

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Hlavní autoři: Simon, Tony J, Wu, Zhongle, Avants, Brian, Zhang, Hui, Gee, James C, Stebbins, Glenn T
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2008
Témata:
Research
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2443161/
https://ncbi.nlm.nih.gov/pubmed/18559106
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1744-9081-4-25
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