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

Type 2N von Willebrand disease mutations in Brazilian individuals.

Haemophilia : the official journal of the World Federation of Hemophilia - 1 Sept 2004

Simon D, Roisenberg I

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 Brazil
Share to Child
Share to Child, Preschool
Share to Heterozygote

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homozygote

Share to Infant

Share to Prevalence

Share to von Willebrand Diseases

Source

Identifiers

PMID: 15357773
DOI: 10.1111/j.1365-2516.2004.00953.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Type 2N von Willebrand disease mutations in Brazilian individuals.PMID 15357773Read ↗

Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biologySemantic proximity Read ↗

Type 2B von Willebrand disease in seven individuals from three different families: phenotypic and genotypic characterization.Semantic proximity Read ↗

Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease.Semantic proximity Read ↗

A standard nomenclature for von Willebrand factor gene mutations and polymorphisms.Semantic proximity Read ↗

Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patients.Semantic proximity Read ↗

Molecular analysis of severe von Willebrand disease in Italian patients.Semantic proximity Read ↗

von Willebrand disease: pathogenesis, classification, and management.Semantic proximity Read ↗

Molecular genetics of von Willebrand diseaseSemantic proximity Read ↗

Genetic heterogeneity of severe von Willebrand disease type III in the German populationSemantic proximity Read ↗

Von Willebrand disease.Semantic proximity Read ↗

Genetic testing for von Willebrand disease: the case for.Semantic proximity Read ↗

Clinical profile of the association of P.R1205h and P.R924q in a patient with von Willebrand's disease.Semantic proximity Read ↗

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