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

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 m...

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Bibliographic Details
Main Authors: Bittel, D, Kibiryeva, N, Talebizadeh, Z, Butler, M
Format: Artigo
Language:Inglês
Published: BMJ Group 2003
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Original Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735542/
https://ncbi.nlm.nih.gov/pubmed/12920063
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.40.8.568
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