Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer.

Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer.

The common single-nucleotide polymorphism (SNP) rs3802842 at 11q23.1 has recently been reported to be associated with risk of colorectal cancer (CRC). To examine this association in detail we genotyped rs3802842 in eight independent case-control series comprising a total of 10 638 cases and 10 457 h...

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Үндсэн зохиолчид: Pittman, A, Webb, E, Carvajal-Carmona, L, Howarth, K, Bernardo, D, Broderick, P, Spain, S, Walther, A, Price, A, Sullivan, K, Twiss, P, Fielding, S, Rowan, A, Jaeger, E, Vijayakrishnan, J, Chandler, I, Penegar, S, Qureshi, M, Lubbe, S, Domingo, E, Kemp, Z, Barclay, E, Wood, W, Martin, L, Gorman, M
Формат: Journal article
Хэл сонгох:English
Хэвлэсэн: 2008

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