The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome

Keyphrases

• Kallmann Syndrome 100%
• Hypogonadotropic Hypogonadism 100%
• Digenic mutation 100%
• PROKR2 20%
• Kiss1 10%
• KAL1 10%
• TAC3 10%
• Intolerant 10%
• Fibroblast Growth Factor Receptor 1 (FGFR1) 10%
• TACR3 10%
• WDR11 10%
• CHD7 10%
• Gene mutation 10%
• Molecular Analysis 10%
• Orthologs 10%
• Monogenic Etiology 10%
• Academic Medical Centers 10%
• Heterozygous mutation 10%
• Gonadotropin-releasing Hormone Receptor (GnRHR) 10%
• Digenic 10%
• Common Genes 10%
• Gonadotropin-releasing Hormone 10%
• Fgf8 10%
• Polymerase Chain Reaction 10%

Medicine and Dentistry

• Kallmann Syndrome 100%
• Hypogonadotropic Hypogonadism 100%
• Polymerase Chain Reaction 10%
• Orthology 10%
• Fibroblast Growth Factor Receptor 1 10%
• CHD7 10%
• Fibroblast Growth Factor 8 10%

Biochemistry, Genetics and Molecular Biology

• CHD7 33%
• FGF8 33%
• Orthology 33%
• Polymerase Chain Reaction 33%
• GNRHR 33%
• KAL1 Gene 33%
• TAC3 33%