S. Dooley

When is a mutation not a mutation: the case of the c.594-2A>C splice variant in a woman harbouring another BRCA1 mutation in trans

R. Scott, A. Spigelman, C. Meldrum, 2016, Hereditary Cancer in Clinical Practice.

cDNA analysis of the BRCA1 unclassified variant c.5194‐12G>A

C. Meldrum, M. Wong-Brown, M. McPhillips, 2013, Clinical genetics.

Lessons learnt from implementation of a Lynch syndrome screening program for patients with gynaecological malignancy.

S. Fox, R. Scott, A. Gill, 2017, Pathology.

Blood‐based detection of RAS mutations to guide anti‐EGFR therapy in colorectal cancer patients: concordance of results from circulating tumor DNA and tissue‐based RAS testing

S. Fox, H. Friess, R. Scott, 2017, Molecular oncology.

A longitudinal evaluation of performance of automated BCR-ABL1 quantitation using cartridge-based detection system

A. Enjeti, A. Ashraf, P. Rowlings, 2015, Pathology.