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Familial Cancer|October 7, 2022
Barriers to completion of cascade genetic testing: how can we improve the uptake of testing for hereditary breast and ovarian cancer syndrome?Ryan Matthew Kahn, Muhammad Danyal Ahsan, Eloise Chapman-Davis, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|January 11, 2020
Cascading After Peridiagnostic Cancer Genetic Testing: An Alternative to Population-Based ScreeningKenneth Offit, Kaitlyn A Tkachuk, Zsofia K Stadler, et al.
Human Molecular Genetics|March 22, 2021
Sequencing at lymphoid neoplasm susceptibility loci maps six myeloma risk genesRosalie Griffin Waller, Robert J Klein, Joseph Vijai, et al.
Journal of Oncology Practice|February 13, 2018
Practice-Changing Strategies to Deliver Affordable, High-Quality Cancer Care: Summary of an Institute of Medicine WorkshopErin P Balogh, Peter B Bach, Peter D Eisenberg, et al.
European Journal of Human Genetics : EJHG|May 8, 2026
Genomic newborn screening: a scoping review of the field's evolution and associated ethical, legal, and social implicationsGemma L Brown, Loren Walker, Mutiat A Afolabi, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 13, 2010
Susceptibility loci associated with prostate cancer progression and mortalityDavid J Gallagher, Joseph Vijai, Angel M Cronin, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 11, 2002
Rare variants of ATM and risk for Hodgkin's disease and radiation-associated breast cancersKenneth Offit, Shlomit Gilad, Shoshana Paglin, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 27, 2009
Mutations in a gene encoding a midbody kelch protein in familial and sporadic classical Hodgkin lymphoma lead to binucleated cellsStephen J Salipante, Matthew E Mealiffe, Jeremy Wechsler, et al.
American Journal of Medical Genetics. Part A|December 22, 2025
Subclinical Telomere Biology Disorder in Cancer Patients Heterozygous for the RTEL1 R1264H Founder VariantLauren G Banaszak, Elise Fiala, Ozge Ceyhan-Birsoy, et al.
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