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Showing articles 0 to 7 of 7 Filter Applied: gene mutation (Click to remove) Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis UptoDate 2022 Jan, Darras, B.T., 2022 A Teenager with Persistent Headache Neurol 92:e1526-e1531, Hu, Y.,et al, 2019 A Neonate with Micrognathia and Hypotonia Neurol 86:e80-e84, Vawter-Lee, M.M.,et al, 2016 Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker NEJM 328:471-475, Shelbourne,P.,et al, 1993 Brief Report:Reverse Mutation in Myotonic Dystrophy NEJM 328:476-480, Brunner,H.G.,et al, 1993 Genetics and Physiology of the Myotonic Muscle Disorders NEJM 328:482-489, Ptacek,L.J.,et al, 1993 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 Showing articles 0 to 7 of 7