Showing results (141-150 of 318) with videos related to

Sort By:
Pageof 32
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 5, 2013
Communication of genetic test results to family and health-care providers following disclosure of research resultsKristi D Graves, Pamela S Sinicrope, Mary Jane Esplen, et al.
American Journal of Human Genetics|February 4, 2018
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational ApproachesLucia Guidugli, Hermela Shimelis, David L Masica, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 18, 2007
Higher frequency of diploidy in young-onset microsatellite-stable colorectal cancerLisa A Boardman, Ruth A Johnson, Gloria M Petersen, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 1, 1999
Alpha1-antitrypsin deficiency allele carriers among lung cancer patientsP Yang, K A Wentzlaff, J A Katzmann, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|October 30, 2015
Clinicopathologic Risk Factor Distributions for MLH1 Promoter Region Methylation in CIMP-Positive TumorsA Joan Levine, Amanda I Phipps, John A Baron, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2020
Returning genomic results in a Federally Qualified Health Center: the intersection of precision medicine and social determinants of healthGabriel Q Shaibi, Iftikhar J Kullo, Davinder P Singh, et al.
Familial Cancer|December 19, 2015
Determining the familial risk distribution of colorectal cancer: a data mining approachRowena Chau, Mark A Jenkins, Daniel D Buchanan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 10, 2018
Comprehensive annotation of BRCA1 and BRCA2 missense variants by functionally validated sequence-based computational prediction modelsSteven N Hart, Tanya Hoskin, Hermela Shimelis, et al.
Gastroenterology|August 24, 2010
The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer historyFay Kastrinos, Ewout W Steyerberg, Rowena Mercado, et al.
Cancer Research|October 31, 2012
A classification model for BRCA2 DNA binding domain missense variants based on homology-directed repair activityLucia Guidugli, Vernon S Pankratz, Namit Singh, et al.
Pageof 32