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SOX2 anophthalmia syndrome: 12 new cases demonstrating broader phenotype and high frequency of large gene deletions
  1. 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
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Citation

Bakrania P, Robinson DO, Bunyan DJ, et al
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 
October 18, 2007

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