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Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24
  1. Correspondence to:
 Dr S Mansour, South West Thames Regional Genetic Service, St George's Hospital Medical School, Cranmer Terrace, London SW17 0RE, UK;
 smansour{at}sghms.ac.uk
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Citation

Brice G, Mansour S, Bell R, et al
Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

Publication history

  • Accepted April 2, 2002
  • Revised March 28, 2002
  • First published July 1, 2002.
Online issue publication 
April 27, 2016

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