A two-phase case–control study for colorectal cancer genetic susceptibility: candidate genes from chromosomal regions 9q22 and 3q22

BACKGROUND: Colorectal cancer (CRC) is the second cause of cancer-related death in the Western world. Much of the CRC genetic risk remains unidentified and may be attributable to a large number of common, low-penetrance genetic variants. Genetic linkage studies in CRC families have reported addition...

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Detalhes bibliográficos
Main Authors: Abulí, A, Fernández-Rozadilla, C, Giráldez, M D, Muñoz, J, Gonzalo, V, Bessa, X, Bujanda, L, Reñé, J M, Lanas, A, García, A M, Saló, J, Argüello, L, Vilella, À, Carreño, R, Jover, R, Xicola, R M, Llor, X, Carvajal-Carmona, L, Tomlinson, I P M, Kerr, D J, Houlston, R S, Piqué, J M, Carracedo, A, Castells, A, Andreu, M, Ruiz-Ponte, C, Castellví-Bel, S
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2011
Assuntos:
Genetics and Genomics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3171011/
https://ncbi.nlm.nih.gov/pubmed/21811255
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/bjc.2011.296
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