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

All too common: bleeding and genetic variation.

Journal of thrombosis and haemostasis : JTH - 1 Nov 2016

Johnsen J 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 Genetic Variation
Share to Hemorrhage

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 27606572
DOI: 10.1111/jth.13499

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 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

All too common: bleeding and genetic variation.PMID 27606572Read ↗

Influence of genetic background on bleeding phenotype in the tail-tip bleeding model and recommendations for standardization: communication from the SSC of the ISTH.Semantic proximity Read ↗

Bleeding disorders.Semantic proximity Read ↗

New approaches to the genetic study of bleeding diathesis in our center: from sanger to next-generation sequencing.Semantic proximity Read ↗

[Genetics of thrombophilia].Semantic proximity Read ↗

Nomenclature of genetic variants in hemostasis.Semantic proximity Read ↗

Puzzling outcome of the nationwide genetic survey of severe/moderate female haemophilia B in Poland.Semantic proximity Read ↗

Gene of the issue: RUNX1 mutations and inherited bleeding.Semantic proximity Read ↗

Polymorphisms and platelet genotyping: the shape of things to come.Semantic proximity Read ↗

Thromboepidemiology: identifying patients with heritable risk for thrombin-mediated thromboembolic events.Semantic proximity Read ↗

Gene of the issue: GP1BA gene mutations associated with bleeding.Semantic proximity Read ↗

Variable bleeding phenotype in an Amish pedigree with von Willebrand disease.Semantic proximity Read ↗

Phenotyping bleeding.Semantic proximity Read ↗

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