Low birth weight is associated with an increased risk in adult life of type 2 diabetes, hypertension and cardiovascular disease (CVD). The fetal insulin hypothesis postulates that genes involving insulin resistance could effect birth weight and disease in later life (Hattersley, 1999). Besides insulin, there is extensive evidence that insulin-like growth factor-I and -II (IGF-I, IGF-II) play an important role in fetal growth. We hypothesized that minor genetic variation in the IGF-I gene could influence pre- and postnatal growth. Three microsatellite markers located in the IGF-I gene in 124 short children (height
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Arends, N., Johnston, L., Hokken-Koelega, A., Van Duijn, C., De Ridder, M., Savage, M., & Clark, A. (2002). Polymorphism in the IGF-I gene: Clinical relevance for short children born small for gestational age (SGA). Journal of Clinical Endocrinology and Metabolism, 87(6), 2720–2724. https://doi.org/10.1210/jc.87.6.2720