Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism

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Description scholarly article
Author/s

author: Janet E. Hall  Daniel L Metzger  Nelly Pitteloud  Maria A Yialamas  James S Acierno  Moosa Mohammadi  Anna V Eliseenkova  William F. Crowley  Astrid Meysing  Omar A Ibrahimi  Andrew A Dwyer 

Publication date April 10, 2006
Language English
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