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Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.

Thrombosis and haemostasis - 1 Dec 1998

Alatri A, Franchi F, Moia M

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PMID: 9869180

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Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.PMID 9869180Read ↗

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

Homozygous 20210G/A prothrombin gene mutation associated with bilateral iliac vein thrombosis: 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 ↗

Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review.Semantic proximity Read ↗

Inherited thrombophilia: an update.Semantic proximity Read ↗

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

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

Homozygous prothrombin gene mutation and ischemic cerebrovascular disease: a case report.Semantic proximity Read ↗

Eclampsia in a woman homozygous for the prothrombin G20210A mutation.Semantic proximity Read ↗

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

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