Gnrh1 mutations identified in patients with ihh

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Access through your institution Buy or subscribe Bouligand, J. _ et al_. Isolated familial hypogonadotropic hypogonadism and a _GNRH1_ mutation. _N. Engl. J. Med._ 360, 2742–2748 (2009).


Chan, Y. M. _ et al_. _GNRH1_ mutations in patients with idiopathic hypogonadotropic hypogonadism. _Proc. Natl Acad. Sci. USA_ 106, 11703–11708 (2009). This is a preview of subscription


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ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our FAQs * Contact customer support Authors * Sarah Payton View author publications You can also search for this


author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Payton, S. _GNRH1_ mutations identified in patients with IHH. _Nat Rev


Urol_ 6, 467 (2009). https://doi.org/10.1038/nrurol.2009.157 Download citation * Issue Date: September 2009 * DOI: https://doi.org/10.1038/nrurol.2009.157 SHARE THIS ARTICLE Anyone you share


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