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Whole Genome Microarray Analysis of Gene Expression in Prader–Willi Syndrome

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 gene express...

詳細記述

保存先:
書誌詳細
出版年:Am J Med Genet A
主要な著者: Bittel, Douglas C., Kibiryeva, Nataliya, Sell, Susan M., Strong, Theresa V., Butler, Merlin G.
フォーマット: Artigo
言語:Inglês
出版事項: 2007
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5467864/
https://ncbi.nlm.nih.gov/pubmed/17236194
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.31606
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