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Lung function changes in newborn screened infants with Cystic Fibrosis are mild and transient during the first 2 years of life.
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This page is a summary of: Pulmonary function deficits in newborn screened infants with cystic fibrosis managed with standard UK care are mild and transient, European Respiratory Journal, November 2017, European Respiratory Society (ERS),
DOI: 10.1183/13993003.00326-2017.
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