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. Author manuscript; available in PMC: 2017 Jun 1.
Published in final edited form as: Clin Genet. 2016 Jan 25;89(6):669–677. doi: 10.1111/cge.12708

Figure 1.

Figure 1

Ocular phenotypes associated with individuals harboring PAX6 coding mutations (A–C) and those for whom no coding mutations were detected (D–F). Images from individuals with known PAX6 mutations were chosen to facilitate comparison with panels D–F and do not capture the full range of ocular phenotypes observed in individuals with identified mutations of the PAX6 gene. Family ID, upper right; causal sequence variant, lower right.