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Article

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

Human genetics - 1 Jan 1992

Morral N, Girbau E, Zielenski J, Nunes V, Casals T, Tsui L C, Estivill X

Abstract excerpt

We describe a polymorphic microsatellite (IVS17BCA) in intron 17B of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. It consists of an 11 to 20 CA/GT dinucleotide repeat, located 424 bp from exon 17B.

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Source

Identifiers

PMID: 1370810
DOI: 10.1007/BF00197276

Genes

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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Dinucleotide (CA/GT) repeat polymorphism in intron 17B of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.PMID 1370810Read ↗

A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.Semantic proximity Read ↗

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

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

Uniparental inheritance of microsatellite alleles of the cystic fibrosis gene (CFTR): identification of a 50 kilobase deletion.Semantic proximity Read ↗

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

Short direct repeats at the breakpoints of a novel large deletion in the CFTR gene suggest a likely slipped mispairing mechanism.Semantic proximity Read ↗

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Tetranucleotide repeat polymorphism at D17S846 maps within 40 kb of GAS at 17q12-q22.Semantic proximity Read ↗

Identification of six mutations (R31L, 441delA, 681delC, 1461ins4, W1089R, E1104X) in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.Semantic proximity Read ↗

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