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

MspI RSP in exon 42 of the canine von Willebrand factor (VWF) gene.

Animal genetics - 1 Jun 1999

Venta P J, Vidal M

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Deoxyribonuclease HpaII
Share to DNA Primers
Share to Dogs
Share to Exons

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Polymerase Chain Reaction

Share to Polymorphism, Restriction Fragment Length

Share to von Willebrand Factor

Source

Identifiers

PMID: 10442993
DOI: 10.1046/j.1365-2052.1999.00404-5.x

Genes

VWF

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

MspI RSP in exon 42 of the canine von Willebrand factor (VWF) gene.PMID 10442993Read ↗

In silico analysis highlights the copy number variation mechanism responsible for the historically reported VWF exon 42 deletion.Semantic proximity Read ↗

A PCR-RFLP marker in canine von Willebrand factor gene (vWF).Semantic proximity Read ↗

Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient.Semantic proximity Read ↗

Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian origin.Semantic proximity Read ↗

Variation in the VWF gene in Swedish patients with type 1 von Willebrand Disease.Semantic proximity Read ↗

Mutation causing von Willebrand's disease in Scottish Terriers.Semantic proximity Read ↗

Duplication of a methionine within the glycoprotein Ib binding domain of von Willebrand factor detected by denaturing gradient gel electrophoresis in a patient with type IIB von Willebrand disease.Semantic proximity Read ↗

A common VWF exon 28 haplotype in the Turkish population.Semantic proximity Read ↗

Molecular screening for the mutation associated with canine degenerative myelopathy (SOD1:c.118G > A) in German Shepherd dogs in Brazil.Semantic proximity Read ↗

D12S17 and D12S25 identify the same MspI RFLP.Semantic proximity Read ↗

A PvuII polymorphism near exon 2 of the dystrophin gene.Semantic proximity Read ↗

Von Willebrand factor short sequence repeat locus 2 (intron 40) consists of three polymorphic subloci.Semantic proximity Read ↗

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