Callea, M., C. E. Willoughby, F. Camarata-Scalisi, I. Giovannoni, A. Vinciguerra, I. Yavuz, M. Di Stazio, E. Di Iorio, G. Clarich, A. Benettoni, A. Galeotti, and E. Bellacchio. “A c.3037G>A Mutation in FBN1 Gene Causing Marfan Syndrome With an Atypically Severe Phenotype.”. Investigación Clínica, Vol. 58, no. 1, Mar. 2017, https://produccioncientificaluz.org./index.php/investigacion/article/view/29043.