Either your web browser doesn't support Javascript or it is currently turned off. In the latter case, please turn on Javascript support in your web browser and reload this page. Language: English Portuguese. To characterize the main identified mutations on cystic fibrosis transmembrane conductance regulator CFTR in a group of children and adolescents at a cystic fibrosis center and its association with the clinical and laboratorial characteristics. Descriptive cross-sectional study including patients with cystic fibrosis who had two alleles identified with CFTR mutation.

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Genetic and phenotypic traits of children and adolescents with cystic fibrosis in Southern Brazil.

Cerca de 1. Sauerbruch F. In: Sauerbruch F, editor. Barcelona: Labor; Landmark perspective: The iron lung. First practical means of respiratory support. Blood gas analysis and critical care medicine.



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