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

CFTR mutations in Turkish and North African cystic fibrosis patients in Europe: implications for screening.

Genetic testing - 1 Mar 2008

Lakeman Phillis, Gille Johan J P, Dankert-Roelse Jeannette E, Heijerman Harry G M, Munck Anne, Iron Albert, Grasemann Hartmut, Schuster Antje, Cornel Martina C, Ten Kate Leo P

Abstract excerpt

AIMS: To obtain more insight into the variability of the CFTR mutations found in immigrant cystic fibrosis (CF) patients who are living in Europe now, and to estimate the test sensitivity of different frequently used methods of DNA analysis to detect CF carriers or patients among these Turkish or...

Read the complete abstract on PubMed

Topics

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

Share to Africa, Northern
Share to Consanguinity
Share to Cystic Fibrosis Transmembrane Conductance Regulator

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Emigration and Immigration

Share to Genetic Carrier Screening

Share to Neonatal Screening

Share to Parents

Share to Turkey

Source

Identifiers

PMID: 18373402
DOI: 10.1089/gte.2007.0046

Genes

CFTR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18373402-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CFTR mutations in Turkish and North African cystic fibrosis patients in Europe: implications for screening.PMID 18373402Read ↗

Beyond the 10%: Unraveling the genetic diversity in Turkish cystic fibrosis patients not eligible for CFTR modulators.Semantic proximity Read ↗

Mutations of the CFTR gene and novel variants in Turkish patients with cystic fibrosis: 24-years experience.Semantic proximity Read ↗

Exploring Turkey's mosaic of novel variants and complex alleles in cystic fibrosis genetics.Semantic proximity Read ↗

Genotype-phenotype correlation of CFTR variants in cystic fibrosis patients.Semantic proximity Read ↗

Highest heterogeneity for cystic fibrosis: 36 mutations account for 75% of all CF chromosomes in Turkish patientsSemantic proximity Read ↗

Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients.Semantic proximity Read ↗

Cystic fibrosis transmembrane conductance regulator mutation spectrum in patients with cystic fibrosis in Tunisia.Semantic proximity Read ↗

Evaluation of clinical and genetic characteristics of cystic fibrosis patients in the Southeastern Anatolia of Turkey.Semantic proximity Read ↗

Sequencing of the CFTR gene in selected Turkish patients with cystic fibrosis.Semantic proximity Read ↗

Distribution of CFTR mutations in the Czech population: positive impact of integrated clinical and laboratory expertise, detection of novel/de novo alleles and relevance for related/derived populations.Semantic proximity Read ↗

CFTR mutations in the Algerian population.Semantic proximity Read ↗

The Genetic Analysis of Cystic Fibrosis Patients With Seven Novel Mutations in the CFTR Gene in the Central Anatolian Region of Turkey.Semantic proximity Read ↗

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