1. Identification of HESX1 mutations in Kallmann syndrome
Kayce Newbern, B.S., Nithya Natrajan, B.S., Hyung-Goo Kim, Ph.D., Lynn P. Chorich, M.S., Lisa M. Halvorson, M.D., Richard S. Cameron, Ph.D., Lawrence C. Layman, M.D. 
Fertility and Sterility 
Volume 99, Issue 7, Pages (June 2013)
DOI: /j.fertnstert
Copyright © 2013 American Society for Reproductive Medicine Terms and Conditions

2. Figure 1
Predicted open reading frame of human HESX1 compared with orthologous proteins of eight other higher-order species. The two boxed regions represent the highly conserved smaller N-terminal corepressor binding domain and the larger C-terminal homeodomain, respectively. The shaded regions indicate the three HESX1 mutations as identified in the genetic screen of 217 IHH/KS patients.
Fertility and Sterility  , DOI: ( /j.fertnstert )
Copyright © 2013 American Society for Reproductive Medicine Terms and Conditions