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VSX2 in microphthalmia: a novel splice site mutation producing a severe microphthalmia phenotype
  1. Correspondence to Professor Graeme C M Black, Medical Genetics Research Group, Genetic Medicine, St Mary's Hospital, Oxford Road, Manchester M13 9W2, UK; graeme.black{at}manchester.ac.uk
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Citation

Burkitt Wright EMM, Perveen R, Bowers N, et al
VSX2 in microphthalmia: a novel splice site mutation producing a severe microphthalmia phenotype

Publication history

  • Accepted April 24, 2009
  • First published March 9, 2010.
Online issue publication 
March 09, 2010

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