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

[Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].

Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego - 1 Feb 2005

Iwańczak Franciszek, Smigiel Robert, Stawarski Andrzej, Pawłowicz Janina, Stembalska Agnieszka, Mowszet Krystyna, Sasiadek Maria

Abstract excerpt

UNLABELLED: Cystic fibrosis is the most common autosomal recessive genetic defect of one gene CFTR, where a variety of mutations were revealed. Cystic fibrosis is a variable disease and to date the genotype-phenotype correlation is difficult to clarify. The aim of the study was to analyse retrospectively the genotype and phenotype of children with cystic fibrosis and to search the correlation between type of...

Read the complete abstract on PubMed

Topics

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

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 Exocrine Pancreatic Insufficiency

Share to Glucose Intolerance

Share to Leukocytes

Share to Liver Failure

Share to Poland

Source

Identifiers

PMID: 17877132

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

[Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].PMID 17877132Read ↗

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

[Gastrointestinal complications of adult patients with cystic fibrosis].Semantic proximity Read ↗

[Cystic fibrosis transmembrane conductance regulator (CFTR) gene: mutations and clinical phenotypes].Semantic proximity Read ↗

[Genotype-phenotype correlation in a sample of Mexican patients with cystic fibrosis].Semantic proximity Read ↗

[Infantile cholestasis caused by CFTR mutation: case report and literature review].Semantic proximity Read ↗

[Diagnosis of cystic fibrosis in adults].Semantic proximity Read ↗

Diverse genotypical features and impacts on clinical course and severity of cystic fibrosis: early childhood experience.Semantic proximity Read ↗

[Cystic fibrosis from the exocrine pancreatic point of view].Semantic proximity Read ↗

[Cystic fibrosis at a Brazilian center of excellence: clinical and laboratory characteristics of 104 patients and their association with genotype and disease severity].Semantic proximity Read ↗

[Nutrition, cystic fibrosis and the digestive tract].Semantic proximity Read ↗

[A study evaluating the correlation between the phenotype and genotype among 65 cystic fibrosis patients].Semantic proximity Read ↗

Patterns of gastrointestinal disease associated with mutations of CFTR.Semantic proximity Read ↗

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