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bronchiectasis with or without elevated sweat chloride 1, modifier of
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CFTR
Cystic fibrosis transmembrane conductance regulator protein expression in the male excretory duct system during development
Confirming the phylogeny of mammals by use of large comparative sequence data sets
Cystic fibrosis
Case studies in cholera: lessons in medical history and science
Prevalence of deltaF508, G551D, G542X, and R553X mutations among cystic fibrosis patients in the North of Brazil
Structure and function of the CFTR chloride channel
An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton
Cancer Gene Census
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