Zobrazeno 1 - 1
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pro vyhledávání: '"Hai-Lu Ma"'
Publikováno v:
Asian Journal of Andrology, Vol 26, Iss 4, Pp 426-432 (2024)
Fibroblast growth factor receptor 1 (FGFR1) mutations are associated with congenital hypogonadotropic hypogonadism (CHH) through inheritance or spontaneous occurrence. We detected FGFR1 mutations in a Chinese cohort of 210 CHH patients at Peking Unio
Externí odkaz:
https://doaj.org/article/f8e12e0c33064e8ea9f8759bc105d73e
