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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...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Nature Publishing Group
2009
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| Θέματα: | |
| Διαθέσιμο Online: | 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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