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Showing articles 0 to 9 of 9 Filter Applied: genetic linkage (Click to remove) Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis Medicine 70:99-117, Gatti,R.A.,et al, 1991 Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations Neurol 47:1269-1277, Baser,M.E., 1996 DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) JNNP 57:1260-1262, Silander,K.,et al, 1994 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 Central Nervous System Lesions in von Hippel-Lindau Syndrome JNNP 55:898-901, Neumann,H.P.H.,et al, 1992 Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992 Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred Medicine 68:1-29, Lamiell,J.M.,et al, 1989 Showing articles 0 to 9 of 9