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35. Variation in lung function as a marker of adherence to oral and inhaled medication in cystic fibrosis. White H, Shaw N, Denman S, Pollard K, Wynne S, Peckham DG. Eur Respir J; 2017 Mar; 49(3):. PubMed ID: 28275171 [Abstract] [Full Text] [Related]
36. Variability of pulmonary function tests in cystic fibrosis. Cooper PJ, Robertson CF, Hudson IL, Phelan PD. Pediatr Pulmonol; 1990 Mar; 8(1):16-22. PubMed ID: 2405342 [Abstract] [Full Text] [Related]
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