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Annals of Neurology|October 1, 1977
Pedigree testing in Duchenne muscular dystrophyA D Roses, M J Roses, B S Metcalf, et al.Journal of Medical Genetics|December 1, 1985
Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales familiesP S Harper, S Youngman, M A Anderson, et al.Medicine|November 1, 1985
Cardiac involvement in myotonic muscular dystrophyJ R Moorman, R E Coleman, D L Packer, et al.Nature Genetics|April 1, 1992
Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tanglesK Hsiao, S R Dlouhy, M R Farlow, et al.Neurology|November 1, 1989
Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected familyB Ghetti, F Tagliavini, C L Masters, et al.Neurobiology of Disease|March 17, 1999
Sialylated human apolipoprotein E (apoEs) is preferentially associated with neuron-enriched cultures from APOE transgenic miceP T Xu, D Schmechel, H L Qiu, et al.Australian Paediatric Journal|January 1, 1988
Update on the molecular genetics of Duchenne muscular dystrophyT Siddique, R Bartlett, M Pericak-Vance, et al.Journal of Medical Genetics|December 1, 1993
Gametic but not somatic instability of CAG repeat length in Huntington's diseaseM E MacDonald, G Barnes, J Srinidhi, et al.Human Molecular Genetics|March 1, 1995
Genetic heterogeneity of autosomal recessive limb-girdle muscular dystrophy in a genetic isolate (Amish) and evidence for a new locusV Allamand, O Broux, N Bourg, et al.Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1986
Molecular genetics of Huntington's diseaseJ F Gusella, T C Gilliam, R E Tanzi, et al.Pageof 37