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Pulmonary function deficits in newborn screened infants with cystic fibrosis managed with standard UK care are mild and transient

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Figure

Table 1.Comparison of lung function and nutritional outcomes in infants with Cystic Fibrosis and healthy controls at approximately 2 years
Table 2: Comparison of changes (∆) in lung function and nutritional outcomes over time in
Table 3. Proportion of NBS CF infants with ‘normal’ or ‘abnormal’ results on each test occasion, and on more than one test occasion
Figure 1. Lung function across the first two years of life in healthy infants and those with CF
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