TY - JOUR AU - Dode, C; Levilliers, J; Dupont, J M TI - Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome JO - Nat Genet VL - 33 PY - 2003 DO - 10.1038/ng1122 L3 - PubMed-ID: 12627230 SP - 463 EP - 465 N1 - et al. ER -