Time to think again: Cystic fibrosis is not an ?all or none? disease
Author:
Publisher
Wiley
Subject
Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health
Reference20 articles.
1. Cystic Fibrosis Foundation. Patient registry 1996. Annual data report. Bethesda, MD: Cystic Fibrosis Foundation; 1997.
2. Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
3. Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA
4. Nasal application of the cationic liposome DC-Chol:DOPE does not alter ion transport, lung function or bacterial growth
5. Cystic fibrosis
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2. Pulmonary Disease in Cystic Fibrosis;Kendig's Disorders of the Respiratory Tract in Children;2019
3. Diagnosis and Presentation of Cystic Fibrosis;Kendig's Disorders of the Respiratory Tract in Children;2019
4. Cystic fibrosis;Nature Reviews Disease Primers;2015-05-14
5. From lip to lab: salty tasting skin is the main clue that raises clinical suspicion of cystic fibrosis in young infants;Acta Paediatrica;2015-03-12
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