Clinical and functional characteristics of a novel heterozygous mutation of the IGF1R gene and IGF1R haploinsufficiency due to terminal 15q26.2->qter deletion in patients with intrauterine growth retardation and postnatal catch-up growth failure - Choi, JH; Kang, M; Kim, GH (J Clin Endocrinol Metab, 2011)
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