The development of cognitive control in children with chromosome 22q11.2 deletion syndrome

Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is caused by the most common human microdeletion, and it is associated with cognitive impairments across many domains. While impairments in cognitive control have been described in children with 22q11.2DS, the nature and development of these impairmen...

Descripción completa

Detalles Bibliográficos
Autores principales: Shapiro, Heather M., Tassone, Flora, Choudhary, Nimrah S., Simon, Tony J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Psychology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4050531/
https://www.ncbi.nlm.nih.gov/pubmed/24959159
http://dx.doi.org/10.3389/fpsyg.2014.00566

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4050531/
https://www.ncbi.nlm.nih.gov/pubmed/24959159
http://dx.doi.org/10.3389/fpsyg.2014.00566

Ejemplares similares