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Pittman, AM;
Webb, E;
Carvajal-Carmona, L;
Howarth, K;
di Bernardo, MC;
Broderick, P;
Spain, S;
Walther, A;
Price, A;
Sullivan, K;
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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;
Thomas, H;
Peto, J;
Bishop, T;
Gray, R;
Maher, ER;
Lucassen, A;
Kerr, D;
Evans, GR;
van Wezel, T;
Morreau, H;
Wijnen, JT;
Hopper, JL;
Southey, MC;
Giles, GG;
Severi, G;
Castellvi-Bel, S;
Ruiz-Ponte, C;
Carracedo, A;
Castells, A;
Forsti, A;
Hemminki, K;
Vodicka, P;
Naccarati, A;
Lipton, L;
Ho, JWC;
Cheng, KK;
Sham, PC;
Luk, J;
Agundez, JAG;
Ladero, JM;
de la Hoya, M;
Caldes, T;
Niitymaki, I;
Tuupanen, S;
Karhu, A;
Aaltonen, LA;
Cazier, JB;
Tomlinson, IPM;
Houlston, RS;
(2008)
Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer.
Human molecular genetics, 17 (23).
pp. 3720-3727.
ISSN 0964-6906
DOI: https://doi.org/10.1093/hmg/ddn267
Full text not available from this repository.