Fig. 1From: Genetic characterization of Italian patients with Bardet-Biedl syndrome and correlation to ocular, renal and audio-vestibular phenotype: identification of eleven novel pathogenic sequence variantsPrevalence of known vs the novel BBS1, BBS2, BBS10 alleles in our genotyped BBS patients. Bars indicate, for the three groups of patients (BBS1, BBS2, BBS10), the percentage of independent alleles with new (dark grey), known (intermediate grey), normal alleles (light grey)Back to article page