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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Udgivet i:Mol Reprod Dev
Main Authors: Wan, Emily S., Qiu, Weiliang, Morrow, Jarrett, Beaty, Terri H., Hetmanski, Jacqueline, Make, Barry J., Lomas, David A., Silverman, Edwin K., DeMeo, Dawn L.
Format: Artigo
Sprog:Inglês
Udgivet: 2015
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Article
Online adgang: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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