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First description of germline mosaicism in familial hypertrophic cardiomyopathy.
Forissier JF, Richard P, Briault S, Ledeuil C, Dubourg O, Charbonnier B, Carrier L, Moraine C, Bonne G, Komajda M, Schwartz K, Hainque B. Forissier JF, et al. Among authors: dubourg o. J Med Genet. 2000 Feb;37(2):132-4. doi: 10.1136/jmg.37.2.132. J Med Genet. 2000. PMID: 10662815 Free PMC article.
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: dubourg o. Genet Couns. 1997;8(2):107-14. Genet Couns. 1997. PMID: 9219008
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy.
Flavigny J, Richard P, Isnard R, Carrier L, Charron P, Bonne G, Forissier JF, Desnos M, Dubourg O, Komajda M, Schwartz K, Hainque B. Flavigny J, et al. Among authors: dubourg o. J Mol Med (Berl). 1998 Mar;76(3-4):208-14. doi: 10.1007/s001090050210. J Mol Med (Berl). 1998. PMID: 9535554
381 results