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Linglart, A, Menguy, C, Couvineau, A, Auzan, C, Gunes, Y, Cancel, M, et al. Recurrent <i>PRKAR1A<\/i> mutation in acrodysostosis with hormone resistance. N Engl J Med 2011;364: 2218\u201326.","DOI":"10.1056\/NEJMoa1012717"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2. Michot, C, Le Goff, C, Goldenberg, A, Abhyankar, A, Klein, C, Kinning, E, et al. Exome sequencing identifies <i>PDE4D<\/i> mutations as another cause of acrodysostosis. Am J Hum Genet 2012;90: 740\u20135.","DOI":"10.1016\/j.ajhg.2012.03.003"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Linglart, A, Fryssira, H, Hiort, O, Holterhus, PM, Perez de Nanclares, G, Argente, J, et al. <i>PRKAR1A<\/i> and <i>PDE4D<\/i> mutations cause acrodysostosis but two distinct syndromes with or without GPCR-signaling hormone resistance. J Clin Endocrinol Metab 2012;97: E2328\u201338.","DOI":"10.1210\/jc.2012-2326"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. 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Online Mendelian Inheritance in Man. Available at: http:\/\/omim.org\/clinicalSynopsis\/101800 (accessed November 3, 2016)."},{"key":"8","unstructured":"8. Jones, KL, Jones, MC, Campo, MD. Smith\u2019s recognizable patterns of human malformation. 7<sup>th<\/sup> ed. Philadelphia: Elsevier Saunders; 2013. p.586-7."},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Nagasaki, K, Asami, T, Kikuchi, T, Uchiyama, M. Longitudinal growth of the short bones of the hand in a girl with pseudohypoparathyroidism type Ia. Clin Pediatr Endocrinol 2007;16: 23\u20139.","DOI":"10.1297\/cpe.16.23"},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Wilson, LC, Oude Luttikhuis, ME, Baraitser, M, Kingston, HM, Trembath, RC. Normal erythrocyte membrane Gs alpha bioactivity in two unrelated patients with acrodysostosis. J Med Genet 1997;34: 133\u20136.","DOI":"10.1136\/jmg.34.2.133"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Clayton, PE, Cianfarani, S, Czernichow, P, Johannsson, G, Rapaport, R, Rogol, A. Management of the child born small for gestational age through to adulthood: a consensus statement of the International Societies of Pediatric Endocrinology and the Growth Hormone Research Society. J Clin Endocrinol Metab 2007;92: 804\u201310.","DOI":"10.1210\/jc.2006-2017"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Fujita, K, Nagasaka, M, Iwatani, S, Koda, T, Kurokawa, D, Yamana, K, et al.Prevalence of small for gestation age (SGA) and short stature in children born SGA who qualify for growth hormone treatment at 3 years of age: Population-based study. Pediatr Intl 2016; 58: 372-6.","DOI":"10.1111\/ped.12859"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Zabransky, S. Fetal growth restriction: definitions, causes, and epidemiology. In: Zabransky S, editor. Caring for children born small for gestational age. 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