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...

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Detalhes bibliográficos
Main Authors: Shapiro, Heather M., Tassone, Flora, Choudhary, Nimrah S., Simon, Tony J.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2014
Assuntos:
Psychology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4050531/
https://ncbi.nlm.nih.gov/pubmed/24959159
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fpsyg.2014.00566
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