Dizygotic twin sisters with normosmic idiopathic hypogonadotropic hypogonadism caused by an FGFR1 gene variant
Author:
Publisher
Korean Society of Pediatric Endocrinology
Subject
Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health
Link
http://e-apem.org/upload/pdf/apem-1938148-074.pdf
Reference20 articles.
1. The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism
2. New insights in the genetics of isolated hypogonadotropic hypogonadism
3. Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism
4. Clinical, endocrinological, and molecular characterization of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism: a single center experience
5. Genetic basis and variable phenotypic expression of Kallmann syndrome: towards a unifying theory
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A Novel FGFR1 Mutation Causing Familial Normosmic Hypogonadotropic Hypogonadism in Three Sisters;The Journal of Obstetrics and Gynecology of India;2024-06-13
2. Treatment of congenital hypogonadotropic hypogonadism in male patients;Annals of Pediatric Endocrinology & Metabolism;2022-09-30
3. Congenital hypogonadotropic hypogonadism: from clinical characteristics to genetic aspects;Precision and Future Medicine;2021-09-30
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