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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...
Tallennettuna:
| Päätekijät: | , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2014
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| Aiheet: | |
| Linkit: | 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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