Clinical Characteristics and Spermatogenesis in Patients with Congenital Hypogonadotropic Hypogonadism Caused by FGFR1 Mutations

OBJECTIVE: The aim of this study was to investigate the clinical characteristics of patients diagnosed with congenital hypogonadotropic hypogonadism (CHH) caused by FGFR1 (fibroblast growth factor receptor 1) gene mutations and to evaluate the effect of gonadotropin or pulsatile gonadotropin-releasi...

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Dettagli Bibliografici
Pubblicato in:Int J Endocrinol
Autori principali: Li, Shuying, Zhao, Yaling, Nie, Min, Ma, Wanlu, Wang, Xi, Ji, Wen, Yang, Yufan, Hao, Ming, Yu, Bingqing, Gao, Yinjie, Mao, Jiangfeng, Wu, Xueyan
Natura: Artigo
Lingua:Inglês
Pubblicazione: Hindawi 2020
Soggetti:
Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7737440/
https://ncbi.nlm.nih.gov/pubmed/33354214
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/8873532
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