Associated Papers
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
Correlation Analysis of Genotypes and Phenotypes in Chinese Male Pediatric Patients With Congenital Hypogonadotropic Hypogonadism.
Wang Y et al.
Frontiers in Endocrinology, 2022
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
Clinical and genetic features of 64 young male paediatric patients with congenital hypogonadotropic hypogonadism.
Wang Y et al.
Clinical Endocrinology, 2017
Integrated analysis of germline and somatic variants in ovarian cancer.
Kanchi KL et al.
Nature Communications, 2014
24448499 (PubMed )
Supplement: NIHMS551112-supplement-9.xlsx › S_Data_8
Fgf17: A regulator of the mid/hind brain boundary in mammals.
Oberholzer Z et al.
Differentiation; Research in Biological Diversity, 0
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