Klinefelter syndrome as a window on the etiology of language and communication impairments in children: the neuroligin-neuroexin hypothesis

Klinefelter syndrome as a window on the etiology of language and communication impairments in children: the neuroligin-neuroexin hypothesis

Aim: To compare the phenotype in Klinefelter syndrome (KS) with (a) specific language impairment (SLI) and (b) 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 ba...

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Bibliografische gegevens
Hoofdauteurs:	Bishop, D, Scerif, G
Formaat:	Journal article
Taal:	English
Gepubliceerd in:	Wiley-Blackwell 2011
Onderwerpen:	Paediatrics Autism Neurogenetics Clinical genetics Neuropsychology Language disorder

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