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Your search keyword '"Gruber, S.B."' showing total 2 results
Start Over Author "Gruber, S.B." Topic ashkenazim -- diseases
2 results on '"Gruber, S.B."'

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

Author

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., and Ellis, N.A.

Subjects
Colorectal cancer -- Genetic aspects, Genetic disorders -- Research, Familial diseases -- Research, Gene mutations -- Health aspects, Ashkenazim -- Genetic aspects, Ashkenazim -- Diseases, Biological sciences
Published
2002

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