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October 1, 1998Endocrine ReviewsOpen Access

Gonadotropin-Releasing Hormone Deficiency in the Human (Idiopathic Hypogonadotropic Hypogonadism and Kallmann’s Syndrome): Pathophysiological and Genetic Considerations

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Authors

SSStephanie B. SeminaraMassachusetts General HospitalFHFrances J. HayesUniversity College DublinWCWilliam F. CrowleyGeological Survey of Ireland

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Cite This Study

Seminara et al. (1998) studied this question.

synapsesocial.com/papers/6a7d65dd5abb11132737d094https://doi.org/10.1210/edrv.19.5.0344
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Also Consider

Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1FERTILE EUNUCH SYNDROME VERSUS CLASSIC HYPOGONADOTROPHIC HYPOGONADISM1978 · 43 citations
  2. 2Genetic Heterogeneity Evidenced by Low Incidence of KAL-1 Gene Mutations in Sporadic Cases of Gonadotropin-Releasing Hormone Deficiency11997 · 101 citations