Enter your terms above and click the 'Search' button.

Showing articles 0 to 10 of 10 Filter Applied: genetic linkage (Click to remove) Molecular Genetic Advances in Fragile X Syndrome J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993 Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl Clin genet 37:355-362, Clarke,J.T.,et al, 1990 Genetic Factors in Alzheimer's Disease:A Review of Recent Advances Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996 DNA Diagnosis of Neurofibromatosis 2:Altered Coding Sequence of the Merlin Tumor Suppressor in an Extended Pedigree JAMA 270:2316-2320, MacCollin,M.,et al, 1993 Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992 Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis Medicine 70:99-117, Gatti,R.A.,et al, 1991 Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence NEJM 325:1720-1738, Sutherland,G.R.,et al, 1991 Prion Dementia Without Characteristic Pathology Lancet 336:7-9, 21-221990., Collinge,J.,et al, 1990 Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis Lancet 2:15-17, Collinge,J.,et al, 1989 Retinitis Pigmentosa Surv Ophthalmol 33:137-177, Pagon,R.A., 1988 Showing articles 0 to 10 of 10