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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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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2003
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| Assuntos: | |
| Acesso em linha: | 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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