A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndrome

BACKGROUND: Chromosome 22q11.2 deletion syndrome (22q11.2DS) results from a 1.5- to 3-megabase deletion on the long arm of chromosome 22 and occurs in approximately 1 in 4000 live births. Previous studies indicate that children with 22q11.2DS are impaired on tasks involving spatial attention. Howeve...

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Detalles Bibliográficos
Autores principales: Shapiro, Heather M, Takarae, Yukari, Harvey, Danielle J, Cabaral, Margarita H, 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/PMC3374293/
https://www.ncbi.nlm.nih.gov/pubmed/22958432
http://dx.doi.org/10.1186/1866-1955-4-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374293/
https://www.ncbi.nlm.nih.gov/pubmed/22958432
http://dx.doi.org/10.1186/1866-1955-4-5

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