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

A polymorphism in the 5' region of coagulation factor VII gene (F7) caused by an inserted decanucleotide.

Human genetics - 1 Jan 1993

Marchetti G, Patracchini P, Papacchini M, Ferrati M, Bernardi F

Abstract excerpt

We describe a polymorphism in the 5' region of the coagulation factor VII (FVII) gene, originating from a decanucleotide (CCTATATCCT) insert present in the less frequent allele. This marker can be detected by restriction analysis of polymerase chain reaction products.

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Base Sequence
Share to DNA

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Transposable Elements

Share to Gene Frequency

Share to Molecular Sequence Data

Share to Polymorphism, Genetic

Share to Promoter Regions, Genetic

Source

Identifiers

PMID: 8381388
DOI: 10.1007/BF00217463

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A polymorphism in the 5' region of coagulation factor VII gene (F7) caused by an inserted decanucleotide.PMID 8381388Read ↗

Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7).Semantic proximity Read ↗

Twenty two novel mutations of the factor VII gene in factor VII deficiency.Semantic proximity Read ↗

The decanucleotide insertion/deletion polymorphism in the promoter region of the coagulation factor VII gene and the risk of familial myocardial infarction.Semantic proximity Read ↗

Using a minigene approach to characterize a novel splice site mutation in human F7 gene causing inherited factor VII deficiency in a Chinese pedigree.Semantic proximity Read ↗

The decanucleotide polymorphism in the factor VII promoter predicts factor VII plasma levels but not the risk of acute coronary syndromes.Semantic proximity Read ↗

Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII gene.Semantic proximity Read ↗

Functional analysis of the genetic variability in the F7 gene promoter.Semantic proximity Read ↗

Promoter methylation in coagulation <i>F7</i> gene influences plasma FVII concentrations and relates to coronary artery diseaseSemantic proximity Read ↗

An NcoI polymorphism in the human complement component 7 (C7) gene.Semantic proximity Read ↗

A polymorphic cluster in the 5' region of the human coagulation factor VII gene: detection, frequency, and linkage disequilibrium.Semantic proximity Read ↗

Novel aberrant splicings caused by a splice site mutation (IVS1a+5g>a) in F7 gene.Semantic proximity Read ↗

Identification of the nucleotide substitution that generates the fourth polymorphic site in human deoxyribonuclease I (DNase I).Semantic proximity Read ↗

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