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Article

Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.

American journal of medical genetics - 1 Apr 1993

Nicholls R D

Abstract excerpt

Although Angelman (AS) and Prader-Willi (PWS) syndromes are human genetic disorders with distinctly different developmental and neurobehavioural phenotypes, they both have abnormalities in inheritance of chromosome 15q11-q13. Whether AS or PWS arises depends on the parental origin of a deletion or uniparental disomy (the inheritance of 2 copies of a genetic locus from only one parent) for 15q11-q13. Normal...

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Identifiers

PMID: 8388169
DOI: 10.1002/ajmg.1320460106

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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