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pubmed-article:17179725pubmed:abstractTextCurrently known mutations account for less than 15% of cases with normosmic hypogonadotropic hypogonadism (nIHH). The objective of the study was to identify novel hereditary associations in the pathogenesis of nIHH.lld:pubmed
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pubmed-article:17179725pubmed:articleTitleMolecular genetic analysis of normosmic hypogonadotropic hypogonadism in a Turkish population: identification and detailed functional characterization of a novel mutation in the gonadotropin-releasing hormone receptor gene.lld:pubmed
pubmed-article:17179725pubmed:affiliationDivision of Paediatric Endocrinology and Metabolism, Cukurova University, Faculty of Medicine, Adana, Turkey. ktopaloglu@cu.edu.trlld:pubmed
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