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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 Medicine (Berlin, Germany)|April 16, 1998
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathyJ Flavigny, P Richard, R Isnard, et al.Journal of Medical Genetics|July 29, 1999
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathyP Richard, R Isnard, L Carrier, et al.Journal of Molecular Biology|December 28, 1999
COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytesJ Flavigny, M Souchet, P Sébillon, 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.European Heart Journal|October 29, 1998
Diagnostic value of electrocardiography and echocardiography for familial hypertrophic cardiomyopathy in genotyped childrenP Charron, O Dubourg, M Desnos, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1997
Penetrance of familial hypertrophic cardiomyopathyP Charron, L Carrier, O Dubourg, et al.Pageof 215