Publication
Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism
Nelly Pitteloud, James S. Acierno Jr., Astrid Meysing, Anna V. Eliseenkova, Jinghong Ma, Omar A. Ibrahimi, Daniel L. Metzger, Frances J. Hayes, Andrew A. Dwyer, Virginia A. Hughes, Maria Yialamas, Janet E. Hall, Ellen Grant, Moosa Mohammadi, William F. Crowley Jr.
Proceedings of the National Academy of Sciences, April 2006, Proceedings of the National Academy of Sciences
DOI: 10.1073/pnas.0600962103