Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome.

Author:

Froggatt N J,Brassett C,Koch D J,Evans D G,Hodgson S V,Ponder B A,Maher E R

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. The tumour spectrum in hereditary non-polyposis colorectal cancer: a study of 24 kindreds in the Netherlands;Vasen, H.F.; Offerhaus, G.J.; den Hartog Jager, F.C.;Int J Cancer,1990

2. Hereditary nonpolyposis colorectal cancer (Lynch syndromes I & II);Lynch, H.T.; Lanspa, S.; Smyrk, T.; Boman, B.; Watson, P.; Lynch, J.;Genetics, pathology, natural history, and cancer control. Part I. Cancer Genet Cytogenet,1991

3. The Lynch syndromes;Lynch, H.T.; Lynch, J.F.;Curr Opin Oncol,1993

4. DT Muir-Torre syndrome: a variant of the cancer family syndrome;Hall, N.R.; Williams, A.T.; Murday, V.A.; Newton, J.A.; Bishop;J Med Genet,1994

5. The mutator gene homolog MSH2 and its association with hereditary nonpolyposis colorectal cancer;Fishel, R.; Lescoe, M.K.; Rao, M.R.S.;Cell,1993

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