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Lance Doucette, Jane Green, Bridget Fernandez, Gordon J Johnson, Patrick Parfrey & Terry-Lynn Young. (2010) A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly. European Journal of Human Genetics 19:3, pages 293-299.
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Nilufer Berker, Yasemin Alanay, Ufuk Elgin, Bilge Volkan-Salanci, Tulay Simsek, Nurten Akarsu & Mehmet Alikasifoglu. (2009) A new autosomal dominant Peters’ anomaly phenotype expanding the anterior segment dysgenesis spectrum. Acta Ophthalmologica 87:1, pages 52-57.
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