Fig. 1From: Homozygosity mapping identified a novel protein truncating mutation (p.Ser100Leufs*24) of the BBS9 gene in a consanguineous Pakistani family with Bardet Biedl syndromeFamily pedigree and facial photographs of patient IV-4 and IV-5. Symbols, tagged with asterisks, indicate individuals selected for genetic analysis in addition to both affected personsBack to article page