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The Lancet. Neurology|July 15, 2026
Parkinson's disease genetics across diverse ancestries: an observational genetic study of causal and risk variants with translational implicationsLara M Lange, Zih-Hua Fang, Mary B Makarious, et al.Pediatric Research|September 10, 2022
Vitamin D deficiency and vitamin D receptor FokI polymorphism as risk factors for COVID-19Nancy M S Zeidan, Hanan M Abd El Lateef, Dalia M Selim, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2018
Expanding the phenome and variome of skeletal dysplasiaSateesh Maddirevula, Saud Alsahli, Lamees Alhabeeb, et al.Cell Reports|January 6, 2015
Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous familiesAnas M Alazami, Nisha Patel, Hanan E Shamseldin, et al.Pageof 18