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Baron, J, S\u00e4vendahl, L, De Luca, F, Dauber, A, Phillip, M, Wit, JM, et al. Short and tall stature: a new paradigm emerges. Nat Rev Endocrinol 2015;11: 735\u201346.","DOI":"10.1038\/nrendo.2015.165"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Roughley, PJ, Mort, JS. The role of aggrecan in normal and osteoarthritic cartilage. J Exp Orthop 2014;1: 8.","DOI":"10.1186\/s40634-014-0008-7"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Tompson, SW, Merriman, B, Funari, VA, Fresquet, M, Lachman, RS, Rimoin, DL, et al. A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C-type lectin domain of aggrecan. Am J Hum Genet 2009;84: 72\u20139.","DOI":"10.1016\/j.ajhg.2008.12.001"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Nilsson, O, Guo, MH, Dunbar, N, Popovic, J, Flynn, D, Jacobsen, C, et al. 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Gkourogianni, A, Andrew, M, Tyzinski, L, Crocker, M, Douglas, J, Dunbar, N, et al.Clinical characterization of patients with autosomal dominant short stature due to aggrecan mutations. J Clin Endocrinol Metab 2016 (e-pub ahead of print 21 Nov 2016;doi: ).","DOI":"10.1210\/jc.2016-3313"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Gleghorn, L, Ramesar, R, Beighton, P, Wallis, G. A mutation in the variable repeat region of the aggrecan gene (AGC1) causes a form of spondyloepiphyseal dysplasia associated with severe, premature osteoarthritis. Am J Hum Genet 2005;77: 484\u201390.","DOI":"10.1086\/444401"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Stattin, EL, Wiklund, F, Lindblom, K, Onnerfjord, P, Jonsson, BA, Tegner, Y, et al. A missense mutation in the aggrecan C-type lectin domain disrupts extracellular matrix interactions and causes dominant familial osteochondritis dissecans. 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