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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Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Bishop, D, Scerif, G
Μορφή: Journal article
Γλώσσα:English
Έκδοση: Wiley-Blackwell 2011
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