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Mutations in FEZF1 Cause Kallmann Syndrome L. Damla Kotan, B. Ian Hutchins, Yusuf Ozkan, Fatma Demirel, Hudson Stoner, Paul J. Cheng, Ihsan Esen, Fatih Gurbuz, Y. Kenan Bicakci, Eda Mengen, Bilgin Yuksel, Susan Wray, A. Kemal Topaloglu The American Journal of Human Genetics Volume 95, Issue 3, Pages 326-331 (September 2014) DOI: 10.1016/j.ajhg.2014.08.006 Copyright © 2014 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 1 The American Journal of Human Genetics 2014 95, 326-331DOI: (10.1016/j.ajhg.2014.08.006) Copyright © 2014 The American Society of Human Genetics Terms and Conditions Terms and Conditions
Figure 2 The American Journal of Human Genetics 2014 95, 326-331DOI: (10.1016/j.ajhg.2014.08.006) Copyright © 2014 The American Society of Human Genetics Terms and Conditions Terms and Conditions
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