We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleLoss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.AuthorsDodé C; Levilliers J; Dupont JM; De Paepe A; Le Dû N; Soussi-Yanicostas N; Coimbra RS; Delmaghani S; Compain-Nouaille S; Baverel F; Pêcheux C; Le Tessier D; Cruaud C; Delpech M; Speleman F; Vermeulen S; Amalfitano A; Bachelot Y; Bouchard P; Cabrol S; Carel JC; Delemarre-van de Waal H; Goulet-Salmon B; Kottler ML; Richard O; Sanchez-Franco F; Saura R; Young J; Petit C; Hardelin JPPublicationNature genetics, 2003, Vol 33, Issue 4, p463ISSN1061-4036Publication typearticleDOI10.1038/ng1122