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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737440/
https://www.ncbi.nlm.nih.gov/pubmed/33354214
http://dx.doi.org/10.1155/2020/8873532

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7737440/
https://www.ncbi.nlm.nih.gov/pubmed/33354214
http://dx.doi.org/10.1155/2020/8873532

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