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Article

An improved method for the detection of the G20210A transition in the prothrombin gene.

Thrombosis research - 1 Dec 1997

Raoul M, Mathonnet F, Peltier J Y, Collet C, Boucly C, Van Amerongen G, Mathieu B, Jaouen E, de Mazancourt P

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PMID: 9556233
DOI: 10.1016/s0049-3848(97)00272-7

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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An improved method for the detection of the G20210A transition in the prothrombin gene.PMID 9556233Read ↗

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

Multiplex PCR for the detection of the factor V Leiden and prothrombin 20210A mutations.Semantic proximity Read ↗

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Clinical and laboratory management of the prothrombin G20210A mutation.Semantic proximity Read ↗

What is the clinical relevance of the prothrombin G20210A mutation?Semantic proximity Read ↗

Multiplex amplification refractory mutation system for the detection of prothrombotic polymorphisms.Semantic proximity Read ↗

Detection of Factor V Leiden and prothrombin c.20210G>A allele by Roche Diagnostics LightCycler®.Semantic proximity Read ↗

Rapid multiplex analysis for the factor V Leiden and prothrombin G20210A mutations associated with hereditary thrombophilia.Semantic proximity Read ↗

Report of a novel kindred with antithrombin heparin-binding site variant (47 Arg to His): demand for an automated progressive antithrombin assay to detect molecular variants with low thrombotic risk.Semantic proximity Read ↗

Multisite study for genotyping of the factor II (prothrombin) G20210A mutation by the invader assay.Semantic proximity Read ↗

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

Sweet's syndrome in a woman with a prothrombin gene (G20210A) mutation.Semantic proximity Read ↗

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