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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Detalles Bibliográficos
Autores principales: Bishop, Dorothy VM, Scerif, Gaia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Psychosocial Aspects
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107947/
https://www.ncbi.nlm.nih.gov/pubmed/21418292
http://dx.doi.org/10.1111/j.1651-2227.2011.02150.x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107947/
https://www.ncbi.nlm.nih.gov/pubmed/21418292
http://dx.doi.org/10.1111/j.1651-2227.2011.02150.x

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