|Title:||Clinical and molecular features of idiopathic hypogonadotropic hypogonadism in Taiwan: A single center experience||Authors:||Cho, Chih-Yi
|Keywords:||Idiopathic hypogonadotropic hypogonadism; Kallmann syndrome; Whole exome sequencing||Issue Date:||25-Mar-2021||Source:||Journal of the Formosan Medical Association = Taiwan yi zhi||Abstract:||
Idiopathic (isolated) hypogonadotropic hypogonadism (IHH) is a rare disease that can be classified as Kallmann syndrome (KS) or normosmic IHH (nIHH). This study investigated the phenotype and genotype of IHH in Taiwanese patients.
|Appears in Collections:||醫學系|
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