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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...
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| Publicado no: | Am J Med Genet A |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | 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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