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Article

Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome.

European journal of pediatrics - 1 Mar 2001

Sipahi T, Duru F, Yarah N, Akar N

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 11277387
DOI: 10.1007/pl00008425

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Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome.PMID 11277387Read ↗

Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene.Semantic proximity Read ↗

Homozygous factor V Leiden mutation in a child with Budd-Chiari syndrome.Semantic proximity Read ↗

Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.Semantic proximity Read ↗

Compound heterozygosity for factor V and methylenetetrahydrofolate reductase mutations in a patient with Budd-Chiari syndrome.Semantic proximity Read ↗

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

Homozygous Factor V Leiden mutation in a child with meningococcal purpura fulminans.Semantic proximity Read ↗

Budd-Chiari syndrome with underlying homozygous factor V Leiden and heterozygous methylenetetrahydrofolate reductase mutations.Semantic proximity Read ↗

Prothrombin gene mutation in Budd-Chiari syndrome-The first case report from India.Semantic proximity Read ↗

Compound heterozygosity involving Antithrombin Cambridge II (p.Ala416Ser) in antithrombin deficiency.Semantic proximity Read ↗

Peculiar laboratory phenotype/ genotype relationship due to compound inherited protein C defects in a child with severe venous thromboembolism.Semantic proximity Read ↗

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