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Human Molecular Genetics|January 1, 1994
A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testingS E Andrew, Y P Goldberg, J Theilmann, et al.Journal of Medical Genetics|August 1, 1994
Apolipoprotein CII-Padova (Tyr37-->stop) as a cause of chylomicronaemia in an Italian kindred from SiculianaS Tuzgöl, S M Bijvoet, T Bruin, et al.Brain Research Bulletin|November 24, 2001
Onset and pre-onset studies to define the Huntington's disease natural historyF Squitieri, M Cannella, P Giallonardo, et al.Nature Genetics|May 1, 1992
Exclusion of DNA changes in the beta-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's diseaseO Riess, A Noerremoelle, C Collins, et al.American Journal of Human Genetics|February 28, 2001
Measurement of mutational flow implies both a high new-mutation rate for Huntington disease and substantial underascertainment of late-onset casesD Falush, E W Almqvist, R R Brinkmann, et al.Cardiorenal Medicine|November 19, 2011
Phosphate Metabolism in Cardiorenal Metabolic DiseaseDeepashree Gupta, Stephen Brietzke, M R Hayden, et al.Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|March 1, 1991
The FDG/PET methodology for early detection of disease onset: a statistical modelC M Clark, W Ammann, W R Martin, et al.Human Genetics|October 1, 1991
Genetic linkage between Huntington disease and the D4S10 locus in South African families: further evidence against non-allelic heterogeneityL J Greenberg, R W Martell, J Theilman, et al.Cell Death and Differentiation|August 4, 2012
Intrinsic cleavage of receptor-interacting protein kinase-1 by caspase-6B J van Raam, D E Ehrnhoefer, M R Hayden, et al.American Journal of Human Genetics|May 1, 1997
The likelihood of being affected with Huntington disease by a particular age, for a specific CAG sizeR R Brinkman, M M Mezei, J Theilmann, et al.Pageof 34