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Article

Phenotypic implications of a co-existent haemorrhagic and thrombotic genotype.

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis - 1 Apr 2012

Thachil Jecko, Martlew Vanessa

Abstract excerpt

Inherited bleeding disorders such as Von Willebrands disease (VWD) present with varying bleeding tendencies in different individuals. There have been several attempts to identify the determinants for this varying severity of the haemorrhagic manifestations, especially in those with milder forms or type 1 VWD. Genetic mutations have been noted in persons with haemophilia to be contributing to a milder bleeding...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22343681
DOI: 10.1097/MBC.0b013e32834fb523

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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.

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