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Article

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

Human mutation - 1 Jan 1992

Parad R B, Gerard C

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Share to Alleles
Share to Base Sequence
Share to Cystic Fibrosis
Share to Cystic Fibrosis Transmembrane Conductance Regulator

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

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Share to Membrane Proteins

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 1284536
DOI: 10.1002/humu.1380010313

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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A sequence variation in intron 17B of the cystic fibrosis transmembrane conductance regulator gene.PMID 1284536Read ↗

Dinucleotide (CA/GT) repeat polymorphism in intron 17B of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.Semantic proximity Read ↗

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Mutations and sequence variations detected in the cystic fibrosis transmembrane conductance regulator (CFTR) gene: a report from the Cystic Fibrosis Genetic Analysis Consortium.Semantic proximity Read ↗

Identification of a 6 bp deletion (3195del6) in exon 17a of the cystic fibrosis (CFTR) gene.Semantic proximity Read ↗

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Novel cystic fibrosis transmembrane conductance regulator variant in a cystic fibrosis patient.Semantic proximity Read ↗

A cluster of cystic fibrosis mutations in exon 17b of the CFTR gene: a site for rare mutations.Semantic proximity Read ↗

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

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

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