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Airways in cystic fibrosis are acidified: detection by exhaled breath condensate
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  1. Correspondence to:
    Dr S Tate, Respiratory Medicine, Ward 54, Anne Ferguson Building, Western General Hospital, Crewe Road South, Edinburgh EH4 2XU, UK;
    steve.tate{at}ed.ac.uk
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Citation

Tate S, MacGregor G, Davis M, et al
Airways in cystic fibrosis are acidified: detection by exhaled breath condensate

Publication history

  • Accepted June 17, 2002
  • Revised May 20, 2002
  • First published November 1, 2002.
Online issue publication 
November 01, 2002

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