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JSES International|July 22, 2024
Identification of rare genetic variants for rotator cuff tearing and repair in high-risk pedigreesRobert Z Tashjian, Michael J Jurynec, Kyle Christy, et al.
The Journal of Urology|May 7, 2016
Inherited Variants in SULT1E1 and Response to Abiraterone Acetate by Men with Metastatic Castration Refractory Prostate CancerNeeraj Agarwal, Anitha B Alex, James M Farnham, et al.
Journal of Dermatological Science|October 30, 2012
Report of a novel OCA2 gene mutation and an investigation of OCA2 variants on melanoma risk in a familial melanoma pedigreeJason E Hawkes, Pamela B Cassidy, Prashiela Manga, et al.
Cancer Control : Journal of the Moffitt Cancer Center|June 14, 2011
Of mice and men: opportunities to use genetically engineered mouse models of synovial sarcoma for preclinical cancer therapeutic evaluationKevin B Jones, Malay Haldar, Joshua D Schiffman, et al.
European Child & Adolescent Psychiatry|March 2, 2023
Efficacy of cannabinoids in neurodevelopmental and neuropsychiatric disorders among children and adolescents: a systematic reviewLauren J Rice, Lisa Cannon, Navin Dadlani, et al.
American Journal of Nephrology|March 25, 2006
A population-based assessment of the familial component of chronic kidney disease mortalityAlexander S Goldfarb-Rumyantzev, Alfred K Cheung, Arsalan N Habib, et al.
BMC Cancer|March 3, 2019
The contribution of the rs55705857 G allele to familial cancer risk as estimated in the Utah population databaseSarah Hummel, Wendy Kohlmann, Thomas M Kollmeyer, et al.
Obstetrics and Gynecology|November 23, 2011
Identification of six loci associated with pelvic organ prolapse using genome-wide association analysisKristina Allen-Brady, Lisa Cannon-Albright, James M Farnham, et al.
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