Associated Papers
A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.
Wang X et al.
Human Molecular Genetics, 2023
Genetic spectrum of Kallmann syndrome: Single-center experience and systematic review.
Patil VA et al.
Clinical Endocrinology, 2022
36138264 (PubMed )
Supplement: supplement_1.xlsx › Sheet1
Mutation profiles and clinical characteristics of Chinese males with isolated hypogonadotropic hypogonadism.
Zhou C et al.
Fertility and Sterility, 2018
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