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Article

Klinefelter syndrome as a window on the aetiology of language and communication impairments in children: the neuroligin-neurexin hypothesis.

Acta paediatrica (Oslo, Norway : 1992) - 1 Jun 2011

Bishop Dorothy V M, Scerif Gaia

Abstract excerpt

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 based on a published survey of children attending a special school. RESULTS: There are close similarities between the...

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Source

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Identifiers

PMID: 21418292
DOI: 10.1111/j.1651-2227.2011.02150.x
PMCID: PMC3107947

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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