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A Millaire

Showing results (91-100 of 95) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesM C Vantyghem, P Pigny, C A Maurage, et al.
Journal of Medical Genetics|August 16, 2003
Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutationsP Sébillon, C Bouchier, L D Bidot, et al.
Circulation|December 15, 1996
Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathyJ F Forissier, L Carrier, H Farza, et al.
Human Mutation|November 26, 1998
Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathyF Tesson, P Richard, P Charron, et al.
European Heart Journal|October 26, 1999
Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE groupP Charron, F Tesson, O Poirier, et al.
Pageof 10

Showing results (91-100 of 95) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 95 results.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesM C Vantyghem, P Pigny, C A Maurage, et al.
Journal of Medical Genetics|August 16, 2003
Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutationsP Sébillon, C Bouchier, L D Bidot, et al.
Circulation|December 15, 1996
Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathyJ F Forissier, L Carrier, H Farza, et al.
Human Mutation|November 26, 1998
Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathyF Tesson, P Richard, P Charron, et al.
European Heart Journal|October 26, 1999
Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE groupP Charron, F Tesson, O Poirier, et al.
Pageof 10