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Article

The 28-kb deletion spanning D15S63 is a polymorphic variant in the Ashkenazi Jewish population.

American journal of human genetics - 1 Jan 2001

Silverstein S, Lerer I, Buiting K, Abeliovich D

Abstract excerpt

D15S63 is one of the loci, on chromosome 15q11-q13, that exhibit parent-of-origin dependent methylation and that is commonly used in the diagnosis of Prader-Willi or Angelman syndromes (PWS/AS). A 28-kb deletion spanning the D15S63 locus was identified in five unrelated patients; in each of them the deletion was inherited from a normal parent. Three of the five families segregating the deletion were reported to...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Chromosomes, Human, Pair 15

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Source

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Identifiers

PMID: 11083946
DOI: 10.1086/316943
PMCID: PMC1234924

Genes

SNRPN

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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