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. 2019 Apr 9;40(5):1285–1317. doi: 10.1210/er.2018-00248

Figure 3.

Figure 3.

Established genetic basis of common genetic variants of pubertal timing, conditions of CHH (IHH and KS), precocious puberty, and delayed puberty and their overlap. Activating and inactivating mutations in Kiss1 and Kiss1R cause the opposite phenotypes, that is, precocious puberty and CHH, respectively. IHH, idiopathic HH.