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Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype
  1. Correspondence to Professor Steve Jeffery, Medical Genetics, St George's, University of London, St George's Hospital Medical School, Cranmer Terrace, London SW17 ORE, UK; sggt100{at}sgul.ac.uk
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Ostergaard P, Simpson MA, Brice G, et al
Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype

Publication history

  • Received September 27, 2010
  • Revised November 2, 2010
  • Accepted November 7, 2010
  • First published January 25, 2011.
Online issue publication 
March 25, 2011

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