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Showing results (261-270 of 347) with videos related to

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Neuromuscular Disorders : NMD|October 10, 2013
Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptomsF L Mastaglia, A Rojana-udomsart, I James, et al.
Journal of Neurogenetics|December 1, 1985
Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophyL H Yamaoka, R J Bartlett, D A Ross, et al.
The Journal of Biological Chemistry|May 16, 2000
Phospholemman is a substrate for myotonic dystrophy protein kinaseJ P Mounsey, J E John, S M Helmke, et al.
American Journal of Human Genetics|August 1, 1987
Familial inheritance of a DXS164 deletion mutation from a heterozygous femaleJ T Lanman, M A Pericak-Vance, R J Bartlett, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1993
Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer diseaseD E Schmechel, A M Saunders, W J Strittmatter, et al.
Annals of Neurology|May 1, 1979
Debrancher deficiency: neuromuscular disorder in 5 adultsS DiMauro, G B Hartwig, A Hays, et al.
Journal of Medical Genetics|August 1, 1989
Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral diseaseT Siddique, H Roper, M A Pericak-Vance, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1993
Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer diseaseW J Strittmatter, K H Weisgraber, D Y Huang, et al.
American Journal of Human Genetics|August 1, 1992
Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, M C Speer, et al.
Genomics|March 20, 1995
The human NACP/alpha-synuclein gene: chromosome assignment to 4q21.3-q22 and TaqI RFLP analysisX Chen, H A de Silva, M J Pettenati, et al.
Pageof 35

Showing results (261-270 of 347) with videos related to

Sort By:
Pageof 35
Neuromuscular Disorders : NMD|October 10, 2013
Polymorphism in the TOMM40 gene modifies the risk of developing sporadic inclusion body myositis and the age of onset of symptomsF L Mastaglia, A Rojana-udomsart, I James, et al.
Journal of Neurogenetics|December 1, 1985
Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophyL H Yamaoka, R J Bartlett, D A Ross, et al.
The Journal of Biological Chemistry|May 16, 2000
Phospholemman is a substrate for myotonic dystrophy protein kinaseJ P Mounsey, J E John, S M Helmke, et al.
American Journal of Human Genetics|August 1, 1987
Familial inheritance of a DXS164 deletion mutation from a heterozygous femaleJ T Lanman, M A Pericak-Vance, R J Bartlett, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 1993
Increased amyloid beta-peptide deposition in cerebral cortex as a consequence of apolipoprotein E genotype in late-onset Alzheimer diseaseD E Schmechel, A M Saunders, W J Strittmatter, et al.
Annals of Neurology|May 1, 1979
Debrancher deficiency: neuromuscular disorder in 5 adultsS DiMauro, G B Hartwig, A Hays, et al.
Journal of Medical Genetics|August 1, 1989
Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral diseaseT Siddique, H Roper, M A Pericak-Vance, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1993
Binding of human apolipoprotein E to synthetic amyloid beta peptide: isoform-specific effects and implications for late-onset Alzheimer diseaseW J Strittmatter, K H Weisgraber, D Y Huang, et al.
American Journal of Human Genetics|August 1, 1992
Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, M C Speer, et al.
Genomics|March 20, 1995
The human NACP/alpha-synuclein gene: chromosome assignment to 4q21.3-q22 and TaqI RFLP analysisX Chen, H A de Silva, M J Pettenati, et al.
Pageof 35