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Cancer Research|May 1, 1993
p53 mutation is a common genetic event in ovarian carcinomaB J Milner, L A Allan, D M Eccles, et al.Journal of Medical Genetics|December 5, 2023
Co-design of patient information leaflets for germline predisposition to cancer: recommendations for clinical practice from the UK Cancer Genetics Group (UKCGG), Cancer Research UK (CRUK) funded CanGene-CanVar Programme and the Association of Genetic Nurse Counsellors (AGNC)Kelly Kohut, Beverley Speight, Julie Young, et al.Oncogene|October 1, 1992
Early loss of heterozygosity on 17q in ovarian cancer. The Abe Ovarian Cancer Genetics GroupD M Eccles, S E Russell, N E Haites, et al.Environmental Pollution (Barking, Essex : 1987)|November 17, 2022
An exploratory spatial contaminant assessment for polar bear (Ursus maritimus) liver, fat, and muscle from northern CanadaV Boutet, M Dominique, K M Eccles, et al.JCO Precision Oncology|September 14, 2020
Pathogenic Variants in CHEK2 Are Associated With an Adverse Prognosis in Symptomatic Early-Onset Breast CancerStephanie L Greville-Heygate, Tom Maishman, William J Tapper, et al.Nature Genetics|November 1, 1994
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2E W Jabs, X Li, A F Scott, et al.American Journal of Human Genetics|December 1, 1996
Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC geneD M Eccles, R van der Luijt, C Breukel, et al.The British Journal of Surgery|May 21, 2015
Family history and outcome of young patients with breast cancer in the UK (POSH study)B K Eccles, E R Copson, R I Cutress, et al.Health Technology Assessment (Winchester, England)|March 23, 2010
North of England and Scotland Study of Tonsillectomy and Adeno-tonsillectomy in Children(NESSTAC): a pragmatic randomised controlled trial with a parallel non-randomised preference studyC Lock, J Wilson, N Steen, et al.Annals of Oncology : Official Journal of the European Society for Medical Oncology|December 19, 2015
Genetic testing in a cohort of young patients with HER2-amplified breast cancerD M Eccles, N Li, R Handwerker, et al.Pageof 30