Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome

BACKGROUND: Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000 live births with a complex and variable presentation that includes medical, socioemotional and psychological symptoms with intellectual impairment. Cognitive impairments in spatiotemporal and visuospatial at...

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Detalles Bibliográficos
Autores principales: Cabaral, Margarita H, Beaton, Elliott A, Stoddard, Joel, Simon, Tony J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374294/
https://www.ncbi.nlm.nih.gov/pubmed/22958454
http://dx.doi.org/10.1186/1866-1955-4-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374294/
https://www.ncbi.nlm.nih.gov/pubmed/22958454
http://dx.doi.org/10.1186/1866-1955-4-6

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