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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Detalles Bibliográficos
Autores principales: Simon, Tony J, Wu, Zhongle, Avants, Brian, Zhang, Hui, Gee, James C, Stebbins, Glenn T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443161/
https://www.ncbi.nlm.nih.gov/pubmed/18559106
http://dx.doi.org/10.1186/1744-9081-4-25

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443161/
https://www.ncbi.nlm.nih.gov/pubmed/18559106
http://dx.doi.org/10.1186/1744-9081-4-25

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