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Klinefelter syndrome as a window on the aetiology of language and communication impairments in children: the neuroligin–neurexin hypothesis
AIM: To compare the phenotype in Klinefelter syndrome (KS) with (i) specific language impairment (SLI) and (ii) XXX and XYY trisomies. METHODS: Phenotypes of KS, XXX and XYY were based on data from a systematic review of neurodevelopmental outcomes plus a recent parent survey. Phenotype of SLI was b...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Publishing Ltd
2011
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3107947/ https://ncbi.nlm.nih.gov/pubmed/21418292 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1651-2227.2011.02150.x |
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