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Showing articles 0 to 9 of 9 Filter Applied: polymerase chain reaction (Click to remove) Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker NEJM 328:471-475, Shelbourne,P.,et al, 1993 Molecular Genetics of Duchenne and Becker Muscular Dystrophy J Pediatr 117:1-15, Darras,B.T., 1990 Rapid Direct Diagnosis of Deletions Carriers of Duchenne and Becker Muscular Dystrophies Lancet 344:302-303, Fassati,A.,et al, 1994 Molecular Genetic Advances in Fragile X Syndrome J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993 Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease) NEJM 329:241-245, Tsujino,S.,et al, 1993 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992 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 Showing articles 0 to 9 of 9