(Q50336618)
Statements
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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. (English)
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Jean-Pierre Hardelin
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Frank Speleman
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Marie-Laure Kottler
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Catherine Dodé
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Jacqueline Levilliers
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Anne De Paepe
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Nathalie Le Dû
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Roney S Coimbra
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Sylvie Compain-Nouaille
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Françoise Baverel
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Christophe Pêcheux
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Dominique Le Tessier
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Corinne Cruaud
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Marc Delpech
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Stefan Vermeulen
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Andrea Amalfitano
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Yvan Bachelot
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Philippe Bouchard
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Sylvie Cabrol
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Jean-Claude Carel
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Henriette Delemarre-van de Waal
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Barbara Goulet-Salmon
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Odile Richard
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Franco Sanchez-Franco
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Robert Saura
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Jacques Young
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10 March 2003
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33
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4
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463-465
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Identifiers
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