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Article

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

European journal of haematology - 1 Jul 2000

Acquila M, Bicocchi M P, Mori P G, Odino S, Valetto A, Bottini F

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Identifiers

PMID: 10914946
DOI: 10.1034/j.1600-0609.2000.9l140.x

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A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy.PMID 10914946Read ↗

The prothrombin 20210 G to A variation and thrombosis.Semantic proximity Read ↗

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Superior sagittal sinus thrombosis in a patient heterozygous for the novel 20210 A allele of the prothrombin gene.Semantic proximity Read ↗

Reliable genotyping of the G-20210-A mutation of coagulation factor II (prothrombin).Semantic proximity Read ↗

Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.Semantic proximity Read ↗

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

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

The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis.Semantic proximity Read ↗

Prothrombin and the prothrombin 20210 G to A polymorphism: their relationship with hypercoagulability and thrombosis.Semantic proximity Read ↗

Coinheritance of factor V Leiden (F5 1691A) and prothrombin 20210 A (F2 20210A) in an Austrian family as cause for early onset of venous thromboembolism.Semantic proximity Read ↗

A three-generation family presenting five cases of homozygosity for the 20210 G to A prothrombin variant.Semantic proximity Read ↗

[20210A mutation of the prothrombin and venous thromboembolism gene].Semantic proximity Read ↗

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