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Array comparative genomic hybridization (aCGH) analysis in Prader–Willi syndrome

✍ Scribed by Merlin G. Butler; William Fischer; Nataliya Kibiryeva; Douglas C. Bittel

Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
194 KB
Volume
146A
Category
Article
ISSN
1552-4825

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## Abstract Prader–Willi syndrome (PWS) is caused by loss of function of paternally expressed genes in the 15q11‐q13 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