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Article

Atypical features in Angelman syndrome due to imprinting defect of uniparental disomy of chromosome 15.

Neuropediatrics - 1 Apr 2000

Dan B, Boyd S G, Christiaens F, Courtens W, Van Maldergem L, Kahn A

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Share to Angelman Syndrome
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Share to Chromosomes, Human, Pair 15
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Identifiers

PMID: 10832589
DOI: 10.1055/s-2000-7485

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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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Atypical features in Angelman syndrome due to imprinting defect of uniparental disomy of chromosome 15.PMID 10832589Read ↗

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[Genetic and clinical study on 17 cases of Angelman syndrome with deletion of 15q11-13].Semantic proximity Read ↗

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