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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.
- Correspondence to: Professor C Inglehearn Vision Research Group, Molecular Medicine Unit, Clinical Sciences Building, St James’s University Hospital, Leeds LS9 7TF, UK; c.inglehearnleeds.ac.uk
Citation
A new phenotype of recessively inherited foveal hypoplasia and anterior segment dysgenesis maps to a locus on chromosome 16q23.2–24.2.
Publication history
- Received March 1, 2004
- Accepted April 6, 2004
- First published October 1, 2004.
Online issue publication
April 27, 2016
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Copyright 2004 Journal of Medical Genetics