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R S Charlton

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Human Mutation|November 25, 2003

Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPAC F Taylor, R S Charlton, J Burn, et al.

British Journal of Cancer|June 27, 2002

Investigations on a clinically and functionally unusual and novel germline p53 mutationJ Rutherford, C E Chu, P M Duddy, et al.

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Search research articles

Showing results (1-10 of 2) with videos related to

Sort By:

Pageof 1

Human Mutation|November 25, 2003

Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrent deletions by MLPAC F Taylor, R S Charlton, J Burn, et al.

British Journal of Cancer|June 27, 2002

Investigations on a clinically and functionally unusual and novel germline p53 mutationJ Rutherford, C E Chu, P M Duddy, et al.

Pageof 1