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Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2023
Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?Jan M Friedman, Yvonne Bombard, Bruce Carleton, et al.
Pediatrics|June 1, 2016
Using Newborn Screening Bloodspots for Research: Public Preferences for Policy OptionsRobin Z Hayeems, Fiona A Miller, Carolyn J Barg, et al.
European Journal of Medical Genetics|November 12, 2021
Challenges and practical solutions for managing secondary genomic findings in primary careAgnes Sebastian, June C Carroll, Meredith Vanstone, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|June 30, 2010
Genome-wide association studies of cancerZsofia K Stadler, Peter Thom, Mark E Robson, et al.
Familial Cancer|March 11, 2014
Mosaic partial deletion of the PTEN gene in a patient with Cowden syndromeErin E Salo-Mullen, Jinru Shia, Isaac Brownell, et al.
Medical Care|March 3, 2010
Geographic access and the use of screening mammographyElena B Elkin, Nicole M Ishill, Jacqueline G Snow, et al.
Journal of Clinical Medicine|August 29, 2024
Innovations in Early Lung Cancer Detection: Tracing the Evolution and Advancements in ScreeningLindsey B Cotton, Peter B Bach, Chris Cisar, et al.
European Journal of Human Genetics : EJHG|May 30, 2025
The development and usability of 'The Genetics Navigator': a digital solution for adult and paediatric clinical genetics servicesSaumeh Saeedi, Daena Hirijkaka, Marc Clausen, et al.
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