Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.

doi:10.1093/hmg/3.10.1877

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Article

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.

Human molecular genetics - 1 Oct 1994

Wevrick R, Kerns J A, Francke U

Abstract excerpt

We have isolated a novel gene from the Prader-Willi syndrome (PWS) smallest region of deletion overlap in proximal human chromosome 15q. IPW (Imprinted gene in the Prader-Willi syndrome region) was isolated using the direct selection method and yeast artificial chromosomes localized to the deleti...

Topics

Alleles
Angelman Syndrome
Base Sequence
Blotting, Northern
Brain
Cell Line
Chromosome Deletion
Chromosome Mapping
Chromosomes, Artificial, Yeast
Chromosomes, Human, Pair 15
DNA Primers
Exons

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Female

Fetus

Fibroblasts

Humans

Lymphocytes

Male

Source

Open in PubMed

Identifiers

PMID: 7849716
DOI: 10.1093/hmg/3.10.1877

Genes

SNRPN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-7849716-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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