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Article

Cystic fibrosis genotype and assessing rates of decline in pulmonary status.

Radiology - 1 Dec 2009

Cleveland Robert H, Zurakowski David, Slattery Dubhfeasa, Colin Andrew A

Abstract excerpt

PURPOSE: To evaluate the hierarchical phenotypic expression of cystic fibrosis transmembrane conductance regulator (CFTR) genotypes in the respiratory system as has been documented in the pancreas. MATERIALS AND METHODS: This study was institutional review board approved; informed consent was not required. HIPAA guidelines were followed. Genotype effects were assessed by using chest radiographic and pulmonary...

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Share to Analysis of Variance
Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Pancreas

Share to Radiography, Thoracic

Share to Regression Analysis

Share to Respiratory Function Tests

Share to Statistics, Nonparametric

Source

Identifiers

PMID: 19952026
DOI: 10.1148/radiol.2533090418

Genes

FEV
CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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