## 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
Genome analysis with gene expression microarrays
β Scribed by Mark Schena
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 641 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0265-9247
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