D. Gareth

Cranial Meningioma in Neurofi bromatosis Type 2 Patients: Role of Mutations

Miriam J. Smith, D. Gareth, R. Evans, 2014 .

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

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

Germline mutations in the neurofibromatosis type 2 tumour suppressor gene.

T. Strachan, D. Bourn, D. Gareth, 1994, Human molecular genetics.

Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families.

A. Craft, M. Santibanez-Koref, P. H. Jones, 1994, Cancer research.

Uptake of genetic testing for cancer predisposition.

D. Craufurd, D. Evans, R. Macleod, 1997, Journal of medical genetics.

Prediction of Breast and Prostate Cancer Risks in Male BRCA1 and BRCA2 Mutation Carriers Using Polygenic Risk Scores

P. Peterlongo, I. Zanna, R. Janavicius, 2017 .

Neurofibromatosis type 2

M. Baser, D. Gareth, G. Evans, 2000 .