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...
| Huvudupphovsmän: | , |
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| Materialtyp: | Journal article |
| Språk: | English |
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Wiley-Blackwell
2011
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