Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes

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author: Stephanie B Seminara  Paul A Boepple  Nelly Pitteloud  Richard Quinton  Pierre Bouloux  Lacey Plummer  James S Acierno  Moosa Mohammadi  William F. Crowley  Astrid Meysing  Andrew A Dwyer 

Publication date June 9, 2006
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