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Showing articles 0 to 6 of 6 Filter Applied: retinopathy (Click to remove) Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Mitochondrial DNA and Disease NEJM 333:638-644, Johns,D.R., 1995 Tamoxifen Retinopathy:A Rare But Serious Complication BMJ 304:495-496, Bentley,C.R.,et al, 1992 Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992 Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA Ann Neurol 26:699-708, Hold,I.J.,et al, 1989 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Showing articles 0 to 6 of 6