Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene

This publication has 20 references indexed in Scilit:

• Two Patients with Cystic Fibrosis, Nonsense Mutations in Each Cystic Fibrosis Gene, and Mild Pulmonary Disease
  New England Journal of Medicine, 1990
• The Relation between Genotype and Phenotype in Cystic Fibrosis — Analysis of the Most Common Mutation (ΔF₅₀₈)
  New England Journal of Medicine, 1990
• A 3′ splice site consensus sequence mutation in the cystic fibrosis gene
  Human Genetics, 1990
• Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer
  Cell, 1990
• A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein
  Nature, 1990
• Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients
  Cell, 1990
• Identification of the Cystic Fibrosis Gene: Genetic Analysis
  Science, 1989
• Age-Related Alterations of Immunoreactive Pancreatic Cationic Trypsinogen in Sera from Cystic Fibrosis Patients with and without Pancreatic Insufficiency
  Pediatric Research, 1986
• Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes
  Cell, 1986
• Colipase and lipase secretion in childhood-onset pancreatic insufficiency
  Gastroenterology, 1984