Showing results (31-40 of 675) with videos related to
Sort By:
Pageof 68
The Journal of Molecular Diagnostics : JMD|March 28, 2009
A rapid and reliable test for BRCA1 and BRCA2 founder mutation analysis in paraffin tissue using pyrosequencingLiying Zhang, Tomas Kirchhoff, Cindy J Yee, et al.Oncology (Williston Park, N.Y.)|July 31, 2010
Genome-wide association studies of cancer: principles and potential utilityZsofia K Stadler, David J Gallagher, Peter Thom, et al.Breast Cancer Research and Treatment|October 14, 2016
Time to incorporate germline multigene panel testing into breast and ovarian cancer patient careRossella Graffeo, Luca Livraghi, Olivia Pagani, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|November 13, 2008
Physicians' experiences with BRCA1/2 testing in community settingsNancy L Keating, Kathryn A Stoeckert, Meredith M Regan, et al.The Journal of Sexual Medicine|October 15, 2014
Addressing sexual dysfunction after risk-reducing salpingo-oophorectomy: effects of a brief, psychosexual interventionSharon L Bober, Christopher J Recklitis, Jennifer Bakan, et al.Cancer Research|August 20, 2009
Comprehensive molecular analysis of mismatch repair gene defects in suspected Lynch syndrome (hereditary nonpolyposis colorectal cancer) casesJames Mueller, Isabella Gazzoli, Prathap Bandipalliam, et al.Clinical Colorectal Cancer|October 6, 2010
Diagnosing hereditary colorectal cancerDavid J Gallagher, James D Smith, Kenneth Offit, et al.Advances in Experimental Medicine and Biology|March 19, 2016
Genomic Biomarkers for Breast Cancer RiskMichael F Walsh, Katherine L Nathanson, Fergus J Couch, et al.Journal of the National Cancer Institute|July 5, 2006
Effect of Factor V Leiden and prothrombin G20210-->A mutations on thromboembolic risk in the national surgical adjuvant breast and bowel project breast cancer prevention trialNeil Abramson, Joseph P Costantino, Judy E Garber, et al.Journal of Genetic Counseling|January 26, 2019
Trans-counseling: A case series of transgender individuals at high risk for BRCA1 pathogenic variantsRosalba E Sacca, Diane R Koeller, Huma Q Rana, et al.Pageof 68