Figure 4From: A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32 Schematic of the linkage region. Overlap of the linkage region in this family with the mapped Volkmann Cataract region is shown along with the location of other genes causing cataract phenotypes (PEX14, EPHA2 and GALE)Back to article page