The founder mutation MSH2*1906G [right arrow] C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population

Authors :: Foulkes, W.D.
Thiffault, I.
Gruber, S.B.
Horwitz, M.
Hamel, N.
Lee, C.
Shia, J.
Markowitz, A.
Figer, A.
Friedman, E.
Farber, D.
Greenwood, C.M. T.
Bonner, J.D.
Nafa, K.
Walsh, T.
Marcus, V.
Tomsho, L.
Gebert, J.
Macrae, F.A.
Gaff, C.L.
Bressac-de Paillerets, B.
Gregersen, P.K.
Weitzel, J.N.
Gordon, P.H.
MacNamara, E.
King, M.-C.
Hampel, H.
de la Chapelle, A.
Boyd, J.
Offit, K.
Rennert, G.
Chong, G.
Ellis, N.A.
Source :: American Journal of Human Genetics. Dec, 2002, Vol. 71 Issue 6, p1395, 18 p.
Publication Year :: 2002

Subjects :: Colorectal cancer -- Genetic aspects
Genetic disorders -- Research
Familial diseases -- Research
Gene mutations -- Health aspects
Ashkenazim -- Genetic aspects
Ashkenazim -- Diseases
Biological sciences

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