## Abstract PraderβWilli syndrome (PWS) is caused by loss of function of paternally expressed genes in the 15q11βq13 region and a paucity of data exists on transcriptome variation. To further characterize genetic alterations in this classic obesity syndrome using whole genome microarrays to analyze
Analysis of whole genome biomarker expression in blood and brain
β Scribed by Brandi Rollins; Maureen V. Martin; Ling Morgan; Marquis P. Vawter
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 556 KB
- Volume
- 9999B
- Category
- Article
- ISSN
- 1552-4841
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