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Article

Identification of mosaicism in Prader-Willi syndrome using fluorescent in situ hybridization.

American journal of medical genetics - 30 Dec 1996

Mowery-Rushton P A, Hanchett J M, Zipf W B, Rogan P K, Surti U

Abstract excerpt

We report on our findings of 4 patients with mosaicism for a deletion of chromosome 15, most commonly associated with Prader-Willi syndrome (PWS). We examined a series of typical and atypical PWS patients in order to identify cytogenetically undetected deletions, using fluorescence in situ hybridization. In 4 of the patients analyzed we detected a deletion in 14-60% of peripheral blood leukocytes, using four...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 8989457
DOI: 10.1002/(SICI)1096-8628(19961230)66:4<403::AID-AJMG4>3.0.CO;2-L

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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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