טוען...
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer
We conducted a genome-wide SNP association study on prostate cancer on over 23,000 Icelanders, followed by a replication study including over 15,500 individuals from Europe and the United States. Two newly identified variants were shown to be associated with prostate cancer: rs5945572 on Xp11.22 and...
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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פורמט: | Artigo |
שפה: | Inglês |
יצא לאור: |
2008
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גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3598012/ https://ncbi.nlm.nih.gov/pubmed/18264098 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.89 |
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