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European Journal of Medical Genetics|March 4, 2017
Identification of a novel CNTNAP1 mutation causing arthrogryposis multiplex congenita with cerebral and cerebellar atrophyShenela Lakhani, Ryan Doan, Mariam Almureikhi, et al.Neuromuscular Disorders : NMD|May 24, 2020
Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients' cohort from Qatar. A population specific founder variantAlice Abdel Aleem, Mahmoud F Elsaid, Nader Chalhoub, et al.Journal of Infection and Public Health|June 15, 2021
COVID-19 versus SARS: A comparative reviewAhmed S Keshta, Saad I Mallah, Khaled Al Zubaidi, et al.Pageof 2