Mutations and polymorphisms in the gonadotrophin genes; clinical relevance
Author:
Affiliation:
1. Physiology
2. Biotechnology, University of Turku, 20520 Turku, Finland
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1365-2265.1998.00454.x
Reference47 articles.
1. Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
2. Isolated follicle‐stimulating hormone deficiency in men: successful long‐term gonadotropin therapy;Al‐Ansari A.A.‐K.;Fertility and Sterility,1984
3. Hypogonadism in a Male with Immunologically Active, Biologically Inactive Luteinizing Hormone: An Exception to a Venerable Rule*
4. Hypogonadism in a Male with an Immunologically Active, Biologically Inactive Luteinizing Hormone: Characterization of the Abnormal Hormone*
5. Bioactivity of gonadotropins;Beitins I.Z.;Endocrine and Metabolic Clinics of North America,1991
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