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Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis
  1. Correspondence to:
 Dr P D Turnpenny, Department of Clinical Genetics, Royal Devon and Exeter Hospital, Exeter EX2 5DW, UK; 
 Peter.Turnpenny{at}rdehc-tr.swest.nhs.uk
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Citation

Turnpenny PD, Whittock N, Duncan J, et al
Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis

Publication history

  • Accepted February 11, 2003
  • Revised February 10, 2003
  • First published May 1, 2003.
Online issue publication 
April 27, 2016

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