Show 10 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="DODE, C" or (type exact bookEditor and editor="DODE, C") Add to list Journal Article A1 Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome C DODE, J LEVILLIERS, JM DUPONT, Anne De Paepe (UGent) , N LE DU, N SOUSSI-YANICOSTAS, RS COIMBRA, S DELMAGHANI, S COMPAIN-NOUAILLE, F BAVEREL, et al. (2003) NATURE GENETICS. 33(4). p.463-465