Showing results (71-80 of 126) with videos related to
Sort By:
Pageof 13
Calcified Tissue International|April 6, 2001
Absence of linkage for bone mineral density to chromosome 12q12-14 in the region of the vitamin D receptor geneR Y Zee, R H Myers, M T Hannan, et al.Archives of Neurology|August 1, 1991
Factors associated with slow progression in Huntington's diseaseR H Myers, D S Sax, W J Koroshetz, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 1, 1985
Late onset of Huntington's diseaseR H Myers, D S Sax, M Schoenfeld, et al.Neurology|February 11, 2000
Rate of functional decline in Huntington's disease. Huntington Study GroupK Marder, H Zhao, R H Myers, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|December 18, 2001
Genome-wide linkage analysis of lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure StudyH Coon, M F Leppert, J H Eckfeldt, et al.American Journal of Human Genetics|June 16, 2004
Common variants in the 5' region of the leptin gene are associated with body mass index in men from the National Heart, Lung, and Blood Institute Family Heart StudyY Jiang, J B Wilk, I Borecki, et al.Journal of Neuropathology and Experimental Neurology|November 11, 1991
Decreased neuronal and increased oligodendroglial densities in Huntington's disease caudate nucleusR H Myers, J P Vonsattel, P A Paskevich, et al.Circulation|June 27, 2001
Genetic and environmental contributions to platelet aggregation: the Framingham heart studyC J O'Donnell, M G Larson, D Feng, et al.Movement Disorders : Official Journal of the Movement Disorder Society|August 6, 1999
Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's diseaseO Joost, C A Taylor, C A Thomas, et al.Neurology|March 1, 1994
A clinical genetic study of Parkinson's disease: evidence for dominant transmissionA M Lazzarini, R H Myers, T R Zimmerman, et al.Pageof 13