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(2021) Impact of short stature on quality of life: a systematic literature review. Growth Horm IGF Res 57\u201358: 101392.","DOI":"10.1016\/j.ghir.2021.101392"},{"key":"2","doi-asserted-by":"crossref","unstructured":"2 Allen DB, Cuttler L (2013) Clinical practice. Short stature in childhood\u2014challenges and choices. N Engl J Med 368: 1220\u20131228.","DOI":"10.1056\/NEJMcp1213178"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3 Cohen P, Rogol AD, Deal CL, Saenger P, Reiter EO, et al. (2008) Consensus statement on the diagnosis and treatment of children with idiopathic short stature: a summary of the Growth Hormone Research Society, the Lawson Wilkins Pediatric Endocrine Society, and the European Society for Paediatric Endocrinology Workshop. J Clin Endocrinol Metab 93: 4210\u20134217.","DOI":"10.1210\/jc.2008-0509"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4 LeRoith D, Roberts CT (2003) The insulin-like growth factor system and cancer. 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(2006) Clinical and functional characteristics of the human Arg59Ter insulin-like growth factor i receptor (IGF1R) mutation: implications for a gene dosage effect of the human IGF1R. J Clin Endocrinol Metab 91: 2264\u20132271.","DOI":"10.1210\/jc.2005-2146"},{"key":"11","doi-asserted-by":"crossref","unstructured":"11 Walenkamp MJ, van der Kamp HJ, Pereira AM, Kant SG, van Duyvenvoorde HA, et al. (2006) A variable degree of intrauterine and postnatal growth retardation in a family with a missense mutation in the insulin-like growth factor I receptor. J Clin Endocrinol Metab 91: 3062\u20133070.","DOI":"10.1210\/jc.2005-1597"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12 Kruis T, Klammt J, Galli-Tsinopoulou A, Wallborn T, Schlicke M, et al. (2010) Heterozygous mutation within a kinase-conserved motif of the insulin-like growth factor I receptor causes intrauterine and postnatal growth retardation. 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(2018) Efficacy and safety of growth hormone treatment in Japanese children with small-for-gestational-age short stature in accordance with Japanese guidelines. Clin Pediatr Endocrinol 27: 225\u2013234.","DOI":"10.1297\/cpe.27.225"},{"key":"#cr-split#-21.1","unstructured":"21 Isojima T, Kato N, Ito Y, Kanzaki S, Murata M (2016) Growth standard charts for Japanese children with mean and standard deviation"},{"key":"#cr-split#-21.2","unstructured":"(SD) values based on the year 2000 national survey. Clin Pediatr Endocrinol 25: 71-76."},{"key":"22","doi-asserted-by":"crossref","unstructured":"22 Itabashi K, Miura F, Uehara R, Nakamura Y (2014) New Japanese neonatal anthropometric charts for gestational age at birth. Pediatr Int 56: 702\u2013708.","DOI":"10.1111\/ped.12331"},{"key":"23","unstructured":"23 (2023) Prospects for change: Duplications of 10p. Rare Chromosome Disorder Support Group. Surrey, United Kingdom. https:\/\/rarechromo.org\/media\/information\/Chromosome%2010\/10p%20duplications%20FTNW.pdf accessed on January 11, 2024."},{"key":"24","doi-asserted-by":"crossref","unstructured":"24 Alfonsi M, Palka C, Morizio E, Gatta V, Franchi S, et al. (2012) A new case of pure partial 7q duplication. Cytogenet Genome Res 136: 1\u20135.","DOI":"10.1159\/000334111"},{"key":"25","doi-asserted-by":"crossref","unstructured":"25 Veenma DC, Eussen HJ, Govaerts LC, de Kort SW, Odink RJ, et al. (2010) Phenotype-genotype correlation in a familial IGF1R microdeletion case. J Med Genet 47: 492\u2013498.","DOI":"10.1136\/jmg.2009.070730"},{"key":"26","doi-asserted-by":"crossref","unstructured":"26 Kawashima Y, Takahashi S, Kanzaki S (2012) Familial short stature with IGF-I receptor gene anomaly. Endocr J 59: 179\u2013185.","DOI":"10.1507\/endocrj.EJ11-0258"},{"key":"27","doi-asserted-by":"crossref","unstructured":"27 Okubo Y, Siddle K, Firth H, O\u2019Rahilly S, Wilson LC, et al. (2003) Cell proliferation activities on skin fibroblasts from a short child with absence of one copy of the type 1 insulin-like growth factor receptor (IGF1R) gene and a tall child with three copies of the IGF1R gene. J Clin Endocrinol Metab 88: 5981\u20135988.","DOI":"10.1210\/jc.2002-021080"},{"key":"28","doi-asserted-by":"crossref","unstructured":"28 G\u00f6pel E, Rockstroh D, Pf\u00e4ffle H, Schlicke M, Pozza SB, et al. (2020) A comprehensive cohort analysis comparing growth and GH therapy response in IGF1R mutation carriers and SGA children. J Clin Endocrinol Metab 105: dgz165.","DOI":"10.1210\/clinem\/dgz165"},{"key":"29","doi-asserted-by":"crossref","unstructured":"29 Poot M, Eleveld MJ, van\u2019t Slot R, van Genderen MM, Verrijn Stuart AA, et al. (2007) Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2\u2192qter. 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