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Page 1
Penetrance of familial hypertrophic cardiomyopathy.
Charron P, Carrier L, Dubourg O, Tesson F, Desnos M, Richard P, Bonne G, Guicheney P, Hainque B, Bouhour JB, Mallet A, Feingold J, Schwartz K, Komajda M. Charron P, et al. Among authors: guicheney p. Genet Couns. 1997;8(2):107-14. Genet Couns. 1997. PMID: 9219008
Genotype-phenotype analysis in four families with mutations in beta-myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.
Tesson F, Richard P, Charron P, Mathieu B, Cruaud C, Carrier L, Dubourg O, Lautié N, Desnos M, Millaire A, Isnard R, Hagege AA, Bouhour JB, Bennaceur M, Hainque B, Guicheney P, Schwartz K, Komajda M. Tesson F, et al. Among authors: guicheney p. Hum Mutat. 1998;12(6):385-92. doi: 10.1002/(SICI)1098-1004(1998)12:6<385::AID-HUMU4>3.0.CO;2-E. Hum Mutat. 1998. PMID: 9829907
A mutation in HERG associated with notched T waves in long QT syndrome.
Dausse E, Berthet M, Denjoy I, André-Fouet X, Cruaud C, Bennaceur M, Fauré S, Coumel P, Schwartz K, Guicheney P. Dausse E, et al. Among authors: guicheney p. J Mol Cell Cardiol. 1996 Aug;28(8):1609-15. doi: 10.1006/jmcc.1996.0151. J Mol Cell Cardiol. 1996. PMID: 8877771
Molecular basis of familial cardiomyopathies.
Schwartz K, Carrier L, Guicheney P, Komajda M. Schwartz K, et al. Among authors: guicheney p. Circulation. 1995 Jan 15;91(2):532-40. doi: 10.1161/01.cir.91.2.532. Circulation. 1995. PMID: 7805259 Review. No abstract available.
264 results