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Language and Literacy Development of Children with Williams Syndrome
Children with Williams syndrome, a rare neurodevelopmental disorder caused by deletion of ~25 genes on chromosome 7q11.23, evidence large individual differences in both broad language and reading abilities. Nevertheless, as a group, children with this syndrome show a consistent pattern characterized...
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| Format: | Artigo |
| Jezik: | Inglês |
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2009
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| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3318995/ https://ncbi.nlm.nih.gov/pubmed/22485062 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/TLD.0b013e3181a72044 |
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