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Showing articles 0 to 11 of 11 Filter Applied: cornea,abnormal (Click to remove) Genetic Counseling in Retinitis Pigmentosa MCV Quart 8:283, Noah,V., 1972 Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003 Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease) Neurol 45:1261-1262, Finelli,P.F., 1995 Neurologic Manifestations of Giant Cell Arteritis Am J Med 89:67-72, Reich,K.A.,et al, 1990 Tangier Disease in a Black Patient:An Unusual Clinical Presentation Am J Med 89:105-108, Lo,W.D.,et al, 1990 Anderson-Fabray Disease, A Commonly Missed Diagnosis BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988 Ocular Complications of Tangier Disease Am J Med 83:991-994, Pressley,T.A.,et al, 1987 Ultrastructural, Neurological, & Glycosaminoglycan Abnormalities in Lowe's Syndrome Ann Neurol 16:40-49, Wisniewski,K.E.,et al, 1984 Corneal Opacification in Infancy MCV Quart 8:230, Ching,F., 1972 Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue (Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972 Angiokeratoma Corporis Diffusum Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962 Showing articles 0 to 11 of 11