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Confirmation and further delineation of the SMG9-deficiency syndrome, a rare and severe developmental disorder.
Lecoquierre F, Bonnevalle A, Chadie A, Gayet C, Dumant-Forest C, Renaux-Petel M, Leca JB, Hazelzet T, Brasseur-Daudruy M, Louillet F, Muraine M, Coutant S, Quenez O, Boland A, Deleuze JF, Frebourg T, Goldenberg A, Saugier-Veber P, Guerrot AM, Nicolas G. Lecoquierre F, et al. Among authors: gayet c. Am J Med Genet A. 2019 Nov;179(11):2257-2262. doi: 10.1002/ajmg.a.61317. Epub 2019 Aug 7. Am J Med Genet A. 2019. PMID: 31390136
Familial dilated cardiomyopathy: clinical features in French families.
Mangin L, Charron P, Tesson F, Mallet A, Dubourg O, Desnos M, Benaïsche A, Gayet C, Gibelin P, Davy JM, Bonnet J, Sidi D, Schwartz K, Komajda M. Mangin L, et al. Among authors: gayet c. Eur J Heart Fail. 1999 Dec;1(4):353-61. doi: 10.1016/s1388-9842(99)00047-1. Eur J Heart Fail. 1999. PMID: 10937948 Free article.
[Apical hypertrophic cardiomyopathy].
Trémeau G, Aupetit JF, Buttard P, Chapon P, Gayet C, Milon H. Trémeau G, et al. Among authors: gayet c. Arch Mal Coeur Vaiss. 1996 Oct;89(10):1283-9. Arch Mal Coeur Vaiss. 1996. PMID: 8952826 Review. French.
80 results