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The Journal of Molecular Diagnostics : JMD|November 17, 2022
Evaluating Multiple Next-Generation Sequencing-Derived Tumor Features to Accurately Predict DNA Mismatch Repair StatusRomy Walker, Peter Georgeson, Khalid Mahmood, et al.
Breast Cancer Research : BCR|November 5, 2018
Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC)John L Hopper, Gillian S Dite, Robert J MacInnis, et al.
Genetic Epidemiology|June 4, 2009
Prostate cancer segregation analyses using 4390 families from UK and Australian population-based studiesRobert J MacInnis, Antonis C Antoniou, Rosalind A Eeles, et al.
Journal of Medical Genetics|February 18, 2011
Melanoma risk for CDKN2A mutation carriers who are relatives of population-based case carriers in Australia and the UKAnne E Cust, Mark Harland, Enes Makalic, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|March 1, 2005
Macrophage scavenger receptor 1 999C>T (R293X) mutation and risk of prostate cancerQuesta Hope, Sarah Bullock, Christopher Evans, et al.
American Journal of Human Genetics|April 3, 2012
Rare mutations in XRCC2 increase the risk of breast cancerD J Park, F Lesueur, T Nguyen-Dumont, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 15, 2012
Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort studyAung Ko Win, Joanne P Young, Noralane M Lindor, et al.
Gastroenterology|January 22, 2014
Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancerAung Ko Win, James G Dowty, Sean P Cleary, et al.
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