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CCDC141 Mutations in Idiopathic Hypogonadotropic Hypogonadism.
Turan I, Hutchins BI, Hacihamdioglu B, Kotan LD, Gurbuz F, Ulubay A, Mengen E, Yuksel B, Wray S, Topaloglu AK. Turan I, et al. Among authors: wray s. J Clin Endocrinol Metab. 2017 Jun 1;102(6):1816-1825. doi: 10.1210/jc.2016-3391. J Clin Endocrinol Metab. 2017. PMID: 28324054 Free PMC article.
Mutations in FEZF1 cause Kallmann syndrome.
Kotan LD, Hutchins BI, Ozkan Y, Demirel F, Stoner H, Cheng PJ, Esen I, Gurbuz F, Bicakci YK, Mengen E, Yuksel B, Wray S, Topaloglu AK. Kotan LD, et al. Among authors: wray s. Am J Hum Genet. 2014 Sep 4;95(3):326-31. doi: 10.1016/j.ajhg.2014.08.006. Am J Hum Genet. 2014. PMID: 25192046 Free PMC article.
GnRH, anosmia and hypogonadotropic hypogonadism--where are we?
Forni PE, Wray S. Forni PE, et al. Among authors: wray s. Front Neuroendocrinol. 2015 Jan;36:165-77. doi: 10.1016/j.yfrne.2014.09.004. Epub 2014 Oct 13. Front Neuroendocrinol. 2015. PMID: 25306902 Free PMC article. Review.
634 results