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Article

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

Blood - 1 Sept 1999

Mainardi J R, Pelsma P M, Koning H, van der Meer J, Middeldorp S, Büller H R, Hamulyák K

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 10507841

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

Related research

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Double-homozygosity for factor V Leiden and the prothrombin gene G20210A variant in a young patient with idiopathic venous thrombosis.PMID 10507841Read ↗

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

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 ↗

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

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

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

Factors V Leiden and the prothrombin gene mutation: two common genetic defects associated with thrombosis.Semantic proximity Read ↗

G20210A prothrombin gene mutation in two siblings with cerebral venous thrombosis.Semantic proximity Read ↗

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

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

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

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