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Showing articles 0 to 12 of 12 Filter Applied: molecular genetics (Click to remove) The Nondystrophic Myotonias In Myology, McGraw-Hill, 2nd Ed, Ch49, p1291-13024., Rudel,R.,et al, 1994 Muscular Dystrophies Lancet 394:2025-2038, Mercuri, E.,et al, 2019 Clinicopathologic Conference, Oligdendroglioma II/IV with IDH1 R132H mutation and codelation of 1p and 19q NEJM 375:2381-2389, Case 38-206, 2016 Dystonia in Children and Adolescents: A Systematic Review and a New Diagnostic Algorithm JNNP 86:774-781, Van Egmond, M.E.,et al, 2015 Outcome in Adult Low-Grade Glioma: The Impact of Prognostic Factors and Treatment Neurol 69:1366-1373, Schiff,D.,et al, 2007 Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 Mitochondrial DNA Polymerase-y and Human Disease Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006 Gliomatosis Cerebri: Molecular Pathology and Clinical Course Ann Neurol 52:390-399,389, Herrlinger,U.,et al, 2002 Investigation of Muscle Disease JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996 Hereditary Hemorrhagic Telangiectasia NEJM 333:918-924, Guttmacher,A.E.,et al, 1995 Wilson Disease Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992 Homing in on Wilson's Disease Editorial, Lancet 1:822-8231989., , 1989 Showing articles 0 to 12 of 12