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Gorlin syndrome: the PTCH gene links ocular developmental defects and tumour formation
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  1. Correspondence to: Nicola K Ragge MD, FRCPCH, FRCOphth, Department of Human Anatomy and Genetics, South Parks Road, Oxford OX1 3QX, UK; nicky.raggeanat.ox.ac.uk
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Ragge NK, Salt A, Collin JRO, et al
Gorlin syndrome: the PTCH gene links ocular developmental defects and tumour formation

Publication history

  • Accepted December 9, 2004
  • First published July 15, 2005.
Online issue publication 
July 15, 2005

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