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

[Detection of delta F508 mutation in cystic fibrosis].

Orvosi hetilap - 20 Sept 1992

Fekete G, Váradi A, Pipiras E, Németh K, Réthy L A, Holics K, Ujhelyi R

Abstract excerpt

The common major mutation (delta F508) resulting in the removal of a phenylalanine residue of the cystic fibrosis gene product has been identified in patients with cystic fibrosis in several European countries. The frequency of this mutation was analyzed in 39 Hungarian patients with cystic fibrosis and in some of their relatives. In 43 out of the total 65 persons involved in the study (66.15%), and in 50% of...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Child, Preschool
Share to Cystic Fibrosis

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

Share to Gene Frequency

Share to Homozygote

Share to Infant

Share to Mutation

Source

Identifiers

PMID: 1408077

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

[Detection of delta F508 mutation in cystic fibrosis].PMID 1408077Read ↗

[Analysis of five mutations of cystic fibrosis occurring in the Hungarian population].Semantic proximity Read ↗

[Frequency of mutations and genotypes of the CFTR gene in cystic fibrosis adults in Poland].Semantic proximity Read ↗

[Correlation between phenotype and genotype in a group of patients with cystic fibrosis].Semantic proximity Read ↗

[The spectrum of mutations in the CFTR gene in patients with cystic fibrosis in Slovakia].Semantic proximity Read ↗

[Determination of the frequency of the deltaF508 mutation among newborns in the city of Moscow and evaluation of the frequency of cystic fibrosis in the European part of Russia].Semantic proximity Read ↗

[Frequency of delta F508 mutation in Venezuelan patients with cystic fibrosis].Semantic proximity Read ↗

[Analysis of mutations in the CFTR gene in patients diagnosed with cystic fibrosis in Poland].Semantic proximity Read ↗

[A molecular study of the delta-F508 mutation and genetic analysis of a sample of cystic fibrosis patients].Semantic proximity Read ↗

[The molecular genetics of cystic fibrosis: the delta F508 allele in Mexican families].Semantic proximity Read ↗

[A molecular genetic analysis of the mutations in the exons of the CFTR gene in cystic fibrosis patients in Ukraine].Semantic proximity Read ↗

[Diagnostic value of the deletion of the delta F508 gene in cystic fibrosis].Semantic proximity Read ↗

The occurrence of various non-delta F508 CFTR gene mutations among Hungarian cystic fibrosis patients.Semantic proximity Read ↗

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