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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Detalhes bibliográficos
Publicado no:Int J Endocrinol
Main Authors: Li, Shuying, Zhao, Yaling, Nie, Min, Ma, Wanlu, Wang, Xi, Ji, Wen, Yang, Yufan, Hao, Ming, Yu, Bingqing, Gao, Yinjie, Mao, Jiangfeng, Wu, Xueyan
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2020
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Research Article
Acesso em linha: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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