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Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
BACKGROUND: Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) occurs in approximately 1:4,000 live births with a complex and variable presentation that includes medical, socioemotional and psychological symptoms with intellectual impairment. Cognitive impairments in spatiotemporal and visuospatial at...
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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/PMC3374294/ https://ncbi.nlm.nih.gov/pubmed/22958454 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1866-1955-4-6 |
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