N. Froggatt

发表

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

B. Ponder, D. Evans, S. Hodgson, 1996, Journal of medical genetics.

Microsatellite instability in early onset and familial colorectal cancer.

D. Evans, J. Joyce, E. Maher, 1996, Journal of medical genetics.

A frequent hMSH2 mutation in hereditary non-polyposis colon cancer syndrome

J. Joyce, E. Maher, B. Ponder, 1995, The Lancet.

Genetic linkage analysis in hereditary non-polyposis colon cancer syndrome.

J. Weissenbach, B. Ponder, D. Evans, 1995, Journal of medical genetics.

MSH2 sequence variations and inherited colorectal cancer susceptibility.

D. Evans, J. Joyce, E. Maher, 1996, European journal of cancer.

Low frequency and late occurrence ofp53 anddcc aberrations in colorectal tumours

S. Leveson, R. C. Garner, N. Froggatt, 2005, Journal of Cancer Research and Clinical Oncology.

Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3' APC gene mutation.

R. Scott, D. Evans, R. Trembath, 1996, Human molecular genetics.

A common MSH 2 mutation in English and North American HNPCC families : origin , phenotypic expression , and sex specific di V erences in colorectal cancer

D. Evans, R. Kolodner, D. Bishop, 1999 .

A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer

D. Evans, R. Kolodner, D. Bishop, 1999, Journal of medical genetics.

Molecular genetic analysis of exons 1 to 6 of the APC gene in non‐polyposis familial colorectal cancer

D. Barton, R. Trembath, J. Joyce, 1995, Clinical genetics.