Figure 1 of AlFadhli, Mol Vis 2012; 18:2931-2936.

Figure 1. Pedigree of Kuwaiti family affected by autosomal dominant congenital cataract. Two novel mutations in the crystalline gamma B (CRYGB) gene resulting in three distinct phenotypes were detected. In addition, the novel tri nucleotide polymorphism was detected in three of the family members. The genotype and the resulting phenotype of each affected member are shown. The arrow indicates the proband.