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Showing articles 0 to 6 of 6 Filter Applied: genetic linkage (Click to remove) Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997 DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) JNNP 57:1260-1262, Silander,K.,et al, 1994 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 Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene Lancet 340:987-991, Tienari,P.J.,et al, 1992 Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis Medicine 70:99-117, Gatti,R.A.,et al, 1991 Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity Ann Neurol 29:469-473, Ryan,S.G.,et al, 1991 Showing articles 0 to 6 of 6