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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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Bibliografski detalji
Glavni autori: Bishop, Dorothy VM, Scerif, Gaia
Format: Artigo
Jezik:Inglês
Izdano: Blackwell Publishing Ltd 2011
Teme:
Online pristup: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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