DOI:
10.1055/s-00034917
Kinder- und Jugendmedizin
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References
Choi JH, Kang M, Kim GH. et al
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.
J Clin Endocrinol Metab 2011;
96: E130-134.
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