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

The genotype of a new linked DNA marker, MP6d-9, is related to the clinical course of cystic fibrosis.

Journal of medical genetics - 1 Jan 1990

Gasparini P, Novelli G, Estivill X, Olivieri D, Savoia A, Ruzzo A, Nunes V, Borgo G, Antonelli M, Williamson R

Abstract excerpt

The clinical symptoms of a cohort of cystic fibrosis patients were related to their genotypes using RFLPs shown with MspI and the closely linked DNA marker MP6d-9. In the majority of CF chromosomes, the restriction site for MspI was present, and the genotype 2/2 was found most often in patients w...

Topics

Cystic Fibrosis
Female
Genetic Linkage
Genetic Markers
Genotype
Humans
Italy
Male
Polymorphism, Restriction Fragment Length

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 1968514
DOI: 10.1136/jmg.27.1.17
PMCID: PMC1016873

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-1968514-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

The genotype of a new linked DNA marker, MP6d-9, is related to the clinical course of cystic fibrosis.PMID 1968514Read ↗

Association of MP6d9 Polymorphism with Clinical Variability in Cystic Fibrosis Patients.Semantic proximity Read ↗

Genetic differences in cystic fibrosis patients with and without pancreatic insufficiency. An Italian collaborative study.Semantic proximity Read ↗

Genetic analysis in cystic fibrosis using the amplification refractory mutation system (ARMS): the J3.11 MspI polymorphism.Semantic proximity Read ↗

Linked marker haplotypes and the delta F508 mutation in adults with mild pulmonary disease and cystic fibrosis.Semantic proximity Read ↗

DNA markers near the cystic fibrosis locus: further analysis of the British population.Semantic proximity Read ↗

Correlation of phenotypic and genetic heterogeneity in cystic fibrosis: variability in sweat electrolyte levels contributes to heterogeneity and is increased with the XV-2c/KM19 B haplotype.Semantic proximity Read ↗

Allele frequencies of Mp6D-9 and GATT markers in 32 Turkish cystic fibrosis families.Semantic proximity Read ↗

Genotype and phenotype in cystic fibrosis.Semantic proximity Read ↗

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