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Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD

1 Aug 2003

Abstract excerpt

BACKGROUND: Prader-Willi syndrome (PWS), the most common genetic cause of marked obesity, is caused by genomic imprinting and loss of expression of paternal genes in the 15q11-q13 region. There is a paucity of data examining simultaneous gene expression in this syndrome. METHODS: We generated cDNA microarrays representing 73 non-redundant genes/transcripts from the 15q11-q13 region, the majority within the PWS...

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PMID: 12920063
DOI: 10.1136/jmg.40.8.568

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