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Article

A polymorphism in intron 20 of the CFTR gene.

Nucleic acids research - 11 Oct 1991

Quere I, Guillermit H, Mercier B, Audrezet M P, Ferec C

Abstract excerpt

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Topics

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Share to Base Sequence
Share to Chromosomes, Human, Pair 7
Share to Cystic Fibrosis Transmembrane Conductance Regulator
Share to Introns

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Membrane Proteins

Share to Oligodeoxyribonucleotides

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

Source

Open in PubMed Open full text

Identifiers

PMID: 1717950
DOI: 10.1093/nar/19.19.5453-a
PMCID: PMC328938

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A polymorphism in intron 20 of the CFTR gene.PMID 1717950Read ↗

A novel mutation (G1249R) in exon 20 of the CFTR gene.Semantic proximity Read ↗

G1244V: a novel missense mutation in exon 20 of the CFTR gene in a Bulgarian cystic fibrosis patient.Semantic proximity Read ↗

A novel splice mutation, 4006-1G>A, in intron 21 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.Semantic proximity Read ↗

Missense variation of the CFTR gene codon 507.Semantic proximity Read ↗

Identification of two novel mutations in the CFTR gene: 3007 del G and 3271 + 1 G-->A.Semantic proximity Read ↗

A new missense mutation (R1283M) in exon 20 of the cystic fibrosis transmembrane conductance regulator gene.Semantic proximity Read ↗

A novel missense mutation, S1159F, in exon 19 of the CFTR gene.Semantic proximity Read ↗

A sequence variation in intron 17B of the cystic fibrosis transmembrane conductance regulator gene.Semantic proximity Read ↗

Two novel frame-shift mutations: 977 insA in exon 6B, and 4016 insT in exon 21, of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.Semantic proximity Read ↗

Complex mutation 4114 ATA-->TT in exon 22 of the cystic fibrosis gene CFTR.Semantic proximity Read ↗

A splicing mutation (1898 + 1G-->T) in the CFTR gene causing cystic fibrosis.Semantic proximity Read ↗

A new missense mutation (E92K) in the first transmembrane domain of the CFTR gene causes a benign cystic fibrosis phenotype.Semantic proximity Read ↗

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