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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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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3374293/ https://ncbi.nlm.nih.gov/pubmed/22958432 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1866-1955-4-5 |
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