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Showing articles 0 to 2 of 2 Filter Applied: genetic linkage (Click to remove) Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 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 Showing articles 0 to 2 of 2