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Journal of Molecular and Cellular Cardiology|July 20, 2000
Homozygotes for a R869G mutation in the beta -myosin heavy chain gene have a severe form of familial hypertrophic cardiomyopathyP Richard, P Charron, C Leclercq, et al.
European Heart Journal|October 29, 2000
Epidemiology of desmin and cardiac actin gene mutations in a european population of dilated cardiomyopathyF Tesson, N Sylvius, A Pilotto, et al.
International Journal of Cardiology|June 25, 2003
Accuracy of European diagnostic criteria for familial hypertrophic cardiomyopathy in a genotyped populationP Charron, J F Forissier, M E Amara, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Penetrance of familial hypertrophic cardiomyopathyP Charron, L Carrier, O Dubourg, et al.
European Journal of Heart Failure|August 11, 2000
Familial dilated cardiomyopathy: clinical features in French familiesL Mangin, P Charron, F Tesson, et al.
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