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Article

Molecular markers for diagnosis of Prader-Willi syndrome in thai patients by fish.

The Southeast Asian journal of tropical medicine and public health - 1 Dec 2003

Wiriyaukaradecha Sirilak, Patmasiriwat Pimpicha, Wasant Pornswan, Tantiniti Pornsri

Abstract excerpt

Paternal microdeletion of chromosome 15 at q11-q13 has been reported in 75% of Prader-Willi syndrome (PWS) patients in western countries. Diagnosis of PWS in Thailand is mainly based on clinical observation and, in some cases, confirmed by conventional cytogenetic analysis. Loss of a tiny segment in this region (microdeletion) has made it difficult to discriminate from the normal karyotype. An attempt to solve...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 15

Share to In Situ Hybridization, Fluorescence

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Share to Ribonucleoproteins, Small Nuclear

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Source

Identifiers

PMID: 15115105

Genes

SNRPN
PML

Provenance

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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