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Annals of Neurology|May 1, 1997
Endoglin gene polymorphism as a risk factor for sporadic intracerebral hemorrhageM J Alberts, J P Davis, C Graffagnino, et al.Nature|November 17, 1983
A polymorphic DNA marker genetically linked to Huntington's diseaseJ F Gusella, N S Wexler, P M Conneally, et al.Science (New York, N.Y.)|August 23, 1985
Huntington's disease: two families with differing clinical features show linkage to the G8 probeS E Folstein, J A Phillips, D A Meyers, et al.Nature|September 17, 1987
Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22G A Rouleau, W Wertelecki, J L Haines, et al.The Pharmacogenomics Journal|August 11, 2004
Identification of a pharmacogenetic effect by linkage disequilibrium mappingC-F Xu, K F Lewis, A J Yeo, et al.Journal of Medical Genetics|September 1, 1987
Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8S R Diehl, M Boehnke, F S Collins, et al.Arzneimittel-Forschung|March 1, 1995
Influence of the susceptibility genes apolipoprotein E-epsilon 4 and apolipoprotein E-epsilon 2 on the rate of disease expressivity of late-onset Alzheimer's diseaseA D Roses, A M Saunders, E H Corder, et al.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.Pageof 37