A carregar...
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...
Na minha lista:
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2008
|
Assuntos: | |
Acesso em linha: | 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 |
Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|