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Disease Markers|August 26, 1998
Clues to the function of the tumour susceptibility gene BRCA2S A Gayther, B A PonderMolecular Medicine Today|April 1, 1997
Mutations of the BRCA1 and BRCA2 genes and the possibilities for predictive testingS A Gayther, B A PonderAnnals of Human Genetics|May 1, 1994
Frequent normal allele loss and maternal origin of the mutation shown by DNA homoduplex analysis in a severely affected patient with adenomatous polyposis coliS A Gayther, M Rees, J D DelhantyJournal of Mammary Gland Biology and Neoplasia|May 20, 2000
The genetics of inherited breast cancerS A Gayther, P D Pharoah, B A PonderJournal of Medical Genetics|July 1, 1995
Rapid detection of rare variants and common polymorphisms in the APC gene by PCR-SSCP for presymptomatic diagnosis and showing allele lossS A Gayther, R Sud, D Wells, et al.Journal of Internal Medicine|March 27, 2012
Role of common genetic variants in ovarian cancer susceptibility and outcome: progress to date from the Ovarian Cancer Association Consortium (OCAC)K L Bolton, C Ganda, A Berchuck, et al.Genes, Chromosomes & Cancer|April 3, 2001
Apparent human BRCA1 knockout caused by mispriming during polymerase chain reaction: implications for genetic testingB Kuschel, S A Gayther, D F Easton, et al.American Journal of Human Genetics|March 1, 1996
Rapid detection of regionally clustered germ-line BRCA1 mutations by multiplex heteroduplex analysis. UKCCCR Familial Ovarian Cancer Study GroupS A Gayther, P Harrington, P Russell, et al.Genetic Epidemiology|January 21, 2000
Risk models for familial ovarian and breast cancerA C Antoniou, S A Gayther, J F Stratton, et al.American Journal of Human Genetics|September 16, 1999
The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genesS A Gayther, P Russell, P Harrington, et al.Pageof 4