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Showing articles 0 to 6 of 6 Filter Applied: genetic neurologic disorders (Click to remove) Duane Syndrome & Congential Upper-Limb Anomalies:A Familial Occurrence Arch Neurol 34:174, Okihiro,M.M.,et al, 1977 Maternal Epilepsy & Abnormalities of the Fetus & Newborn Lancet 839, Oct1972., Speidel,B.,et al, 1972 Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis UptoDate 2022 Jan, Darras, B.T., 2022 Myotonic Dystrophy In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994 Dominant Spinopontine Atrophy Arch Neurol 35:156, Pogacar,S.,et al, 1978 Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families Ann Neurol 4:37, Bender,A.N.,et al, 1978 Showing articles 0 to 6 of 6