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Venous thromboembolism in a young woman with combined homozygosity for factor V Leiden and prothrombin G20210A mutations.

Haematologica - 1 Nov 2005

Leonard Marc, Gala Jean Luc, Verschuren Frank, Coche Emmanuel, Deneys Véronique, Hainaut Philippe

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Share to 3' Untranslated Regions
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 16266921

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Venous thromboembolism in a young woman with combined homozygosity for factor V Leiden and prothrombin G20210A mutations.PMID 16266921Read ↗

Chronic thromboembolic pulmonary hypertension in a patient heterozygous for both factor V Leiden and G20210 prothrombin mutation.Semantic proximity Read ↗

Double-homozygosity for factor V Leiden and the prothrombin gene G20210A variant in a young patient with idiopathic venous thrombosis.Semantic proximity Read ↗

Thrombosis in a patient with combined homozygosity for the factor V Leiden mutation and a mutation in the 3'-untranslated region of the prothrombin gene.Semantic proximity Read ↗

Spontaneous superficial vein thrombosis in a young patient double heterozygous for factor V Leiden and the prothrombin G20210A mutation: a case report.Semantic proximity Read ↗

Pregnancy-associated deep vein thrombosis in a double homozygous carrier of factor V Leiden and prothrombin G20210A.Semantic proximity Read ↗

Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.Semantic proximity Read ↗

Combined factor V Leiden and prothrombin genotyping in patients presenting with thromboembolic episodes.Semantic proximity Read ↗

A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy.Semantic proximity Read ↗

Venous thromboembolism at a young age in a brother and sister with coinheritance of homozygous 20210A/A prothrombin mutation and heterozygous 1691G/A factor V Leiden mutation.Semantic proximity Read ↗

The prothrombin gene variant 20210A in venous and arterial thromboembolism.Semantic proximity Read ↗

A further case of homozygous G20210A prothrombin gene mutation without thromboembolic events.Semantic proximity Read ↗

Hepatic vein thrombosis in a patient with mutant prothrombin 20210A allele.Semantic proximity Read ↗

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