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Showing articles 0 to 9 of 9 Filter Applied: genetic linkage (Click to remove) Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations Neurol 47:1269-1277, Baser,M.E., 1996 Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus J Med Genet 32:25-31, Twist,E.C.,et al, 1995 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene NEJM 326:444-449, Medori,R.,et al, 1992 Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992 Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis Medicine 70:99-117, Gatti,R.A.,et al, 1991 Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl Clin genet 37:355-362, Clarke,J.T.,et al, 1990 Showing articles 0 to 9 of 9