Buchan, J. G.; Alvarado, D. M.; Haller, G. E.; Cruchaga, C; Harms, M. B.; Zhang, T; Willing, M. C.; Grange, D. K.; Braverman, A. C.; Miller, N. H.; Morcuende, J. A.; Tang, N. L.; Lam, T. P.; Ng, B. K.; Cheng, J. C.; Dobbs, M. B.; Gurnett, C. A. (2014). „Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis”. Human Molecular Genetics. 23: 5271—5282. PMID24833718. doi:10.1093/hmg/ddu224.
Dietz HC; Guttmacher, Alan E.; Dietz, Harry C. (2010). „New therapeutic approaches to mendelian disorders”. N. Engl. J. Med. 363 (9): 852—63. PMID20818846. doi:10.1056/NEJMra0907180.
Corson GM, Charbonneau NL, Keene DR, Sakai LY (2004). „Differential expression of fibrillin-3 adds to microfibril variety in human and avian, but not rodent, connective tissues”. Genomics. 83 (3): 461—72. PMID14962672. doi:10.1016/j.ygeno.2003.08.023.
Buchan, J. G.; Alvarado, D. M.; Haller, G. E.; Cruchaga, C; Harms, M. B.; Zhang, T; Willing, M. C.; Grange, D. K.; Braverman, A. C.; Miller, N. H.; Morcuende, J. A.; Tang, N. L.; Lam, T. P.; Ng, B. K.; Cheng, J. C.; Dobbs, M. B.; Gurnett, C. A. (2014). „Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis”. Human Molecular Genetics. 23: 5271—5282. PMID24833718. doi:10.1093/hmg/ddu224.
Dietz HC; Guttmacher, Alan E.; Dietz, Harry C. (2010). „New therapeutic approaches to mendelian disorders”. N. Engl. J. Med. 363 (9): 852—63. PMID20818846. doi:10.1056/NEJMra0907180.
Corson GM, Charbonneau NL, Keene DR, Sakai LY (2004). „Differential expression of fibrillin-3 adds to microfibril variety in human and avian, but not rodent, connective tissues”. Genomics. 83 (3): 461—72. PMID14962672. doi:10.1016/j.ygeno.2003.08.023.