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A genome-wide scan of 10 000 gene-centric variants and colorectal cancer risk

Genome scans based on gene-centric single nucleotide polymorphisms (SNPs) have been proposed as an efficient approach to identify disease-causing variants that is complementary to scans based on tagging SNPs. Adopting this approach to identify low-penetrance susceptibility alleles for colorectal can...

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שמור ב:
מידע ביבליוגרפי
Main Authors: Webb, Emily, Broderick, Peter, Lubbe, Steven, Chandler, Ian, Tomlinson, Ian, Houlston, Richard S
פורמט: Artigo
שפה:Inglês
יצא לאור: Nature Publishing Group 2009
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC2986682/
https://ncbi.nlm.nih.gov/pubmed/19471308
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2009.92
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