Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Characterization of 3 microsatellites of the cystic fibrosis gene in Argentine families].

Medicina - 1 Jan 2001

Visich A A, Barreiro C Z, Chertkoff L P

Abstract excerpt

Argentine population is highly heterogeneous for the cystic fibrosis (CF) transmembrane regulator (CFTR) gene mutations. The study of 14 more common mutations identified both mutated alleles in only 51% of patients. This study confirmed the diagnosis of cystic fibrosis in these patients and enabled the detection of asymptomatic carriers in their families. However, in the remaining patients the direct molecular...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Argentina
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 DNA, Satellite

Share to Genetic Linkage

Share to Genetic Markers

Share to Haplotypes

Share to Microsatellite Repeats

Source

Identifiers

PMID: 11265619

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.

Related research

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

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Characterization of 3 microsatellites of the cystic fibrosis gene in Argentine families].PMID 11265619Read ↗

[Molecular diagnosis of cystic fibrosis in 93 Argentinean patients and detection of heterozygotes in affected families. Impact on health services and therapeutic advances].Semantic proximity Read ↗

Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry.Semantic proximity Read ↗

Prenatal diagnosis of cystic fibrosis in a highly heterogeneous population.Semantic proximity Read ↗

Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations.Semantic proximity Read ↗

[Identification of mutation in the gene cystic fibrosis transmembrane regulator (CFTR) in Chilean patients with cystic fibrosis].Semantic proximity Read ↗

Microsatellite haplotypes for cystic fibrosis: mutation frameworks and evolutionary tracers.Semantic proximity Read ↗

Complete screening of the CFTR gene in Argentine cystic fibrosis patients.Semantic proximity Read ↗

Cystic fibrosis in a southern Brazilian population: characteristics of 90% of the alleles.Semantic proximity Read ↗

Analysis of linkage disequilibrium between different cystic fibrosis mutations and three intragenic microsatellites in the Italian population.Semantic proximity Read ↗

[CFTR gene sequencing in a group of Chilean patients with cystic fibrosis].Semantic proximity Read ↗

[Analysis of various polymorphic markers of the CFTR gene in cystic fibrosis patients and healthy donors from the Moscow region].Semantic proximity Read ↗

Three Novel CFTR Polymorphic Repeats Improve Segregation Analysis for Cystic FibrosisSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.