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Genome-wide site-specific differential methylation in the blood of individuals with Klinefelter Syndrome
Klinefelter syndrome (KS) (47 XXY) is a common sex-chromosome aneuploidy with an estimated prevalence of 1 in every 660 male births. Investigations into the associations between DNA methylation and the highly variable clinical manifestations of KS have largely focused on the supernumerary X chromoso...
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| Publicado no: | Mol Reprod Dev |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4439255/ https://ncbi.nlm.nih.gov/pubmed/25988574 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mrd.22483 |
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