1. B. Ergun-Longmire, M.P. Wajnrajch: Growth and Growth Disorders. In: K.R. Feingold, B. Anawalt, A. Boyce, G. Chrousos, W.W. de Herder, K. Dhatariya, K. Dungan, J.M. Hershman, J. Hofland, S. Kalra, G. Kaltsas, C. Koch, P. Kopp, M. Korbonits, C.S. Kovacs, W. Kuohung, B. Laferrère, M. Levy, EA. McGee, R. McLachlan, J.E. Morley, M. New, J. Purnell, R. Sahay, F. Singer, M.A. Sperling, C.A. Stratakis, D.L. Trence, and D.P. Wilson, (eds.) Endotext. MDText.com, Inc., South Dartmouth (MA) (2000).
2. K. Forbes, M. Westwood, The IGF axis and placental function. Horm. Res. Paediatr. 69, 129–137 (2008). https://doi.org/10.1159/000112585
3. R. Peoples, A. Milatovich, U. Francke, Hemizygosity at the insulin-like growth factor I receptor (IGF1R) locus and growth failure in the ring chromosome 15 syndrome. Cytogenet. Cell Genet. 70, 228–234 (1995). https://doi.org/10.1159/000134040
4. P. Prontera, L. Micale, A. Verrotti, V. Napolioni, G. Stangoni, G. Merla, A new homozygous IGF1R variant defines a clinically recognizable incomplete dominant form of SHORT syndrome. Hum. Mutat. 36, 1043–1047 (2015). https://doi.org/10.1002/humu.22853
5. I. Castilla-Cortazar, J.R. de Ita, G.A. Aguirre, F. Castorena-Torres, J. Ortiz-Urbina, M. García-Magariño, R.G. de la Garza, C. Diaz Olachea, M.I. Elizondo Leal, Fanconi anemia and laron syndrome. Am. J. Med. Sci. 353, 425–432 (2017). https://doi.org/10.1016/j.amjms.2017.02.001