Figure 1
From: Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland
Pedigrees of KS patients carrying an FGFR1 or KAL1 mutation. Pedigrees #11, #503, #45, #54, and #50 are consistent with autosomal dominant form of inheritance. X-chromosomal recessive inheritance is apparent in pedigrees #2 and #9.