Ushbu ishga iqtibos qilgan ishlar

2 ta ish

Ish: Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

1. "The significance of the GNRH 1 gene polymorphism (rs 6185, rs1812594) in the development of idiopathic hypogonadotropic hypogonadism."

   Мавлонов У.Х., Yu.М. Urmanova, Khudaybergenov Sh.A +1

   MaqolaHypothalamic control of reproductive hormonesTexas Journal of Medical Science20240 iqtibos

   ABIABI:AkademIndex/openalex/2024.article.004691

2. "Results of Genetic Studies of Adolescents with Idiopathic Hypogonadotropic Hypogonadism"

   Yu.М. Urmanova

   MaqolaGenetics and Physical PerformanceBiomedical Journal of Scientific & Technical Research20240 iqtibos

   ABIABI:AkademIndex/openalex/2024.article.005714