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Article

Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.

American journal of human genetics - 1 Jun 2004

Fernandez Thomas, Morgan Thomas, Davis Nicole, Klin Ami, Morris Ashley, Farhi Anita, Lifton Richard P, State Matthew W

Abstract excerpt

3p deletion syndrome is a rare contiguous-gene disorder involving the loss of the telomeric portion of the short arm of chromosome 3 and characterized by developmental delay, growth retardation, and dysmorphic features. All reported cases have involved, at a minimum, the deletion of chromosome 3 telomeric to the band 3p25.3. Despite the presence of several genes in this region that are involved in neural...

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Share to Cell Adhesion Molecules, Neuronal
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 15106122
DOI: 10.1086/421474
PMCID: PMC1182094

Genes

CNTN4

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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