APA
Humbertclaude V., Hamroun D., Picot M., Bezzou K., Bérard C., Boespflug-Tanguy O., Bommelaer C., Campana-Salort E., Cances C., Chabrol B., Commare M., Cuisset J., de Lattre C., Desnuelle C., Echenne B., Halbert C., Jonquet O., Labarre-Vila A., N'guyen-Morel M., Pages M., Pepin J., Petitjean T., Pouget J., Ollagnon-Roman E., Richelme C., Rivier F., Sacconi S., Tiffreau V., Vuillerot C., Béroud C., Tuffery-Giraud S. & Claustres M. (20140606). [Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]. : Revue neurologique.
Chicago
Humbertclaude V, Hamroun D, Picot M-C, Bezzou K, Bérard C, Boespflug-Tanguy O, Bommelaer C, Campana-Salort E, Cances C, Chabrol B, Commare M-C, Cuisset J-M, de Lattre C, Desnuelle C, Echenne B, Halbert C, Jonquet O, Labarre-Vila A, N'guyen-Morel M-A, Pages M, Pepin J-L, Petitjean T, Pouget J, Ollagnon-Roman E, Richelme C, Rivier F, Sacconi S, Tiffreau V, Vuillerot C, Béroud C, Tuffery-Giraud S and Claustres M. 20140606. [Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]. : Revue neurologique.
Harvard
Humbertclaude V., Hamroun D., Picot M., Bezzou K., Bérard C., Boespflug-Tanguy O., Bommelaer C., Campana-Salort E., Cances C., Chabrol B., Commare M., Cuisset J., de Lattre C., Desnuelle C., Echenne B., Halbert C., Jonquet O., Labarre-Vila A., N'guyen-Morel M., Pages M., Pepin J., Petitjean T., Pouget J., Ollagnon-Roman E., Richelme C., Rivier F., Sacconi S., Tiffreau V., Vuillerot C., Béroud C., Tuffery-Giraud S. and Claustres M. (20140606). [Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]. : Revue neurologique.
MLA
Humbertclaude V, Hamroun D, Picot M-C, Bezzou K, Bérard C, Boespflug-Tanguy O, Bommelaer C, Campana-Salort E, Cances C, Chabrol B, Commare M-C, Cuisset J-M, de Lattre C, Desnuelle C, Echenne B, Halbert C, Jonquet O, Labarre-Vila A, N'guyen-Morel M-A, Pages M, Pepin J-L, Petitjean T, Pouget J, Ollagnon-Roman E, Richelme C, Rivier F, Sacconi S, Tiffreau V, Vuillerot C, Béroud C, Tuffery-Giraud S and Claustres M. [Phenotypic heterogeneity and phenotype-genotype correlations in dystrophinopathies: Contribution of genetic and clinical databases]. : Revue neurologique. 20140606.