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Article

Communicative competence and behavioural phenotype in children with Smith-Magenis syndrome.

Genetic counseling (Geneva, Switzerland) - 1 Jan 2004

Sarimski K

Abstract excerpt

Smith-Magenis syndrome is characterized by a range of minor physical and facial abnormalities and is caused by a de novo deletion on chromosome 17. Most children function in the moderate to severe ranges of mental retardation. Results of a survey on adaptive skills, communicative competence and b...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15517828

Genes

SMS

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15517828-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Communicative competence and behavioural phenotype in children with Smith-Magenis syndrome.PMID 15517828Read ↗

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[Diagnostic difficulties in Smith-Magenis Syndrome (SMS) on the basis of own experience and literature data].Semantic proximity Read ↗

Intellectual and Behavioral Phenotypes of Smith-Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic RAI1 Variant.Semantic proximity Read ↗

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