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Clinical science - Extended reports
SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions
- Miss Nicola Ragge, Dept of Physiology, Anatomy and Genetics, Le Gros Clark Building, South Parks Road, Oxford, OX1 3QX, United Kingdom; nicky.ragge{at}dpag.ox.ac.uk
Citation
SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions
Publication history
- Accepted May 11, 2007
- First published May 23, 2007.
Online issue publication
March 22, 2016
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2007 BMJ Publishing Group Ltd