Associated Papers
A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.
Wang X et al.
Human Molecular Genetics, 2023
Phenotypic and genotypic landscape of PROKR2 in neuroendocrine disorders.
Martinez-Mayer J et al.
Frontiers in Endocrinology, 2023
Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism.
Men M et al.
Molecular Genetics & Genomic Medicine, 2021
Genotypic and phenotypic spectra of FGFR1, FGF8, and FGF17 mutations in a Chinese cohort with idiopathic hypogonadotropic hypogonadism.
Men M et al.
Fertility and Sterility, 2020
Somatic Mutations from Whole Exome Sequencing Analysis of the Patients with Biliary Tract Cancer.
Yoon KA et al.
Genomics & Informatics, 2018
Identification of risk genes in Chinese nonobstructive azoospermia patients based on whole-exome sequencing.
Liu YJ et al.
Asian Journal of Andrology, 0
Genetic variants of G-protein coupled receptors associated with pubertal disorders.
Suzuki E et al.
Reproductive Medicine and Biology, 0
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