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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

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Description scientific article published on 10 March 2003
Author/s

author: Jean-Michel Dupont  Henriette Delemarre-van de Waal  Nadia Soussi-Yanicostas  Marie-Laure Kottler  Sedigheh Delmaghani  Jean-Claude Carel  Christine Petit  Jean-Pierre Hardelin  Frank Speleman 

Publication date March 10, 2003
Language English
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