Gnrh1 mutations identified in patients with ihh

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

content, access via your institution ACCESS OPTIONS Access through your institution Subscribe to this journal Receive 12 print issues and online access $209.00 per year only $17.42 per issue

Learn more Buy this article * Purchase on SpringerLink * Instant access to full article PDF Buy now Prices may be subject to local taxes which are calculated during checkout ADDITIONAL

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

the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer

Nature SharedIt content-sharing initiative