Figure 3.

Pedigree and haplotype map of a three generation family with lens dislocation, glaucoma, and corneal guttae. The proband (II:1) is identified by the arrow and shaded symbols represent affected individuals. Circles are females and squares are males. Segregation of markers D15S1232, D15S659, and D15S648 are shown as well, and individual II:4 underwent a double recombination event leaving him with a normal phenotype.