European journal of heart failure, 23(8), 1276-1286. Wiley DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria instname Restrepo-Cordoba, M A, Wahbi, K, Florian, A R, Jiménez-Jáimez, J, Politano, L, Arad, M, Climent-Paya, V, Garcia-Alvarez, A, Hansen, R B, Larrañaga-Moreira, J M, Kubanek, M, Lopes, L R, Ros, A, Jurcut, R, Rasmussen, T B, Ruiz-Guerrero, L, Pribe-Wolferts, R, Palomino-Doza, J, Bilinska, Z, Rodríguez-Palomares, J F, Van Loon, R L E, Basurte Elorz, M T, Quarta, G, Robledo Iñarritu, M, Verdonschot, J A J, Stojkovic, T, Shomanova, Z, Bermudez-Jimenez, F, Palladino, A, Freimark, D, García-Álvarez, M I, Jorda, P, Dominguez, F, Ochoa, J P, Girolami, F, Brugada, R, Meder, B, Barriales-Villa, R, Mogensen, J, Laforêt, P, Yilmaz, A, Elliott, P, Garcia-Pavia, P & for the European Genetic Cardiomyopathies Initiative Investigators (see online supplementary Appendix S1) 2021, ' Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy ', European Journal of Heart Failure, vol. 23, no. 8, pp. 1276-1286 . https://doi.org/10.1002/ejhf.2250
European Journal of Human Genetics, 25(7), 823-831. Nature Publishing Group Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid Consejería de Sanidad de la Comunidad de Madrid European Journal of Human Genetics, 25, 823-831 European Journal of Human Genetics, 25, 7, pp. 823-831
European Journal of Human Genetics, 23(9), 1176-1185. Nature Publishing Group European Journal of Human Genetics, 23(9), 1176-85. Nature Publishing Group European journal of human genetics, 23(9), 1176-1185. Nature Publishing Group European Journal of Human Genetics, 23(9), 1176. Nature Publishing Group Ockeloen, C W, Willemsen, M H, de Munnik, S, van Bon, B W M, de Leeuw, N, Verrips, A, Kant, S G, Jones, E A, Brunner, H G, van Loon, R L E, Smeets, E E J, van Haelst, M M, van Haaften, G, Nordgren, A, Malmgren, H, Grigelioniene, G, Vermeer, S, Louro, P, Ramos, L, Maal, T J J, van Heumen, C C, Yntema, H G, Carels, C E L & Kleefstra, T 2015, ' Further delineation of the KBG syndrome phenotype caused by ANKRD11 aberrations ', European Journal of Human Genetics, vol. 23, no. 9, pp. 1176-85 . https://doi.org/10.1038/ejhg.2014.253 Europe PubMed Central European Journal of Human Genetics, 23(9), 1176-1185 European Journal of Human Genetics
Ockeloen, C W, Willemsen, M H, de Munnik, S, van Bon, B W M, de Leeuw, N, Verrips, A, Kant, S G, Jones, E A, Brunner, H G, van Loon, R L E, Smeets, E E J, van Haelst, M M, van Haaften, G, Nordgren, A, Malmgren, H, Grigelioniene, G, Vermeer, S, Louro, P, Ramos, L, Maal, T J J, van Heumen, C C, Yntema, H G, Carels, C E L & Kleefstra, T 2015, ' Erratum: Further delineation of the KBG syndrome caused by ANKRD11 aberrations ', European Journal of Human Genetics, vol. 23, no. 9, pp. 1270 . https://doi.org/10.1038/ejhg.2015.130