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Showing articles 0 to 9 of 9 Filter Applied: chromosomal abnormality (Click to remove) Wilson Disease Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992 Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene Brain 129:1674-1684, Horvath, R.,et al, 2006 Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency Neurol 60:1413-1417, Pearl,P.L.,et al, 2003 Dopamine, Dystonia, and the Deficient Co-Factor Lancet 345:1130, Williams,A.C., 1995 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Homing in on Wilson's Disease Editorial, Lancet 1:822-8231989., , 1989 Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987 Prenatal Genetic Diagnosis in 3000 Amniocenteses NEJM 300:157-163, Golbus,M.S.,et al, 1979 Showing articles 0 to 9 of 9