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Article

[Genomic imprinting and its role in Prader-Willi and Angelman syndromes].

Genetika - 1 Dec 1996

Mglinets V A, Levina L Ia, Konstantinova L M

Abstract excerpt

Published and our own data, included in the CHRODYS database, on the dependence of phenotypic abnormalities in mono-, di-, and trisomics at human chromosome 15 on its parental origin are reviewed. The concept is confirmed that Prader-Willi and Angelman syndromes result from the combined effect of gene or chromosome mutations impairing the expression of syndrome-specific genes and from genomic imprinting, i.e.,...

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Share to Chromosomes, Human, Pair 15
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Source

Identifiers

PMID: 9102354

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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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