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Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation
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  1. Correspondence to:
 Professor A Clarke
 Institute of Medical Genetics, Cardiff University, University Hospital of Wales, Cardiff CF14 4XN, UK; clarkeaj{at}cf.ac.uk
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Citation

Archer H, Evans J, Leonard H, et al
Correlation between clinical severity in patients with Rett syndrome with a p.R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation

Publication history

  • Received July 7, 2006
  • Accepted July 12, 2006
  • Revised July 7, 2006
  • First published August 11, 2006.
Online issue publication 
April 27, 2016

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