Genetic Diagnosis of Hypogonadotropic Hypogonadism and Kallmann Syndrome
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Elsevier
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Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience;Annals of Pediatric Endocrinology & Metabolism;2015
2. The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome;Fertility and Sterility;2011-12
3. The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome;Molecular and Cellular Endocrinology;2011-10
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