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A new phenotype of recessively inherited foveal hypoplasia and anterior segment dysgenesis maps to a locus on chromosome 16q23.2–24.2.

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Footnotes

  • * Present address, Department of Anatomy and Cell Biology, University of Bergen, Norway

  • This study was supported by Wellcome Trust Grants 071590 and 073477.

  • Conflicts of interest: none declared

  • The first two authors contributed equally to this work.