Mark Redston

Abnormal TP53 Predicts Risk of Progression in Patients With Barrett’s Esophagus Regardless of a Diagnosis of Dysplasia

A. Bass, M. Redston, A. Noffsinger, 2020, medRxiv.

STK11/LKB1 germline mutations are not identified in most Peutz–Jeghers syndrome patients

Z. Cohen, S. Gallinger, M. Redston, 1999, Clinical genetics.

MSH2 deficient mice are viable and susceptible to lymphoid tumours

H. Griesser, T. Mak, P. Waterhouse, 1995, Nature Genetics.