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Circulation Research|September 19, 1998
Familial hypertrophic cardiomyopathy: from mutations to functional defectsG Bonne, L Carrier, P Richard, et al.
Journal of Molecular and Cellular Cardiology|March 25, 2000
Deletion in the cardiac troponin I gene in a family from northern Sweden with hypertrophic cardiomyopathyS Mörner, P Richard, E Kazzam, et al.
Journal of Medical Genetics|February 9, 2000
First description of germline mosaicism in familial hypertrophic cardiomyopathyJ F Forissier, P Richard, S Briault, et al.
Journal of Medical Genetics|October 4, 2002
Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experienceP Charron, D Héron, M Gargiulo, et al.
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.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Penetrance of familial hypertrophic cardiomyopathyP Charron, L Carrier, O Dubourg, et al.
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