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Article

Combined factor V Leiden and prothrombin genotyping in patients presenting with thromboembolic episodes.

Archives of pathology & laboratory medicine - 1 Jan 2001

Friedline J A, Ahmad E, Garcia D, Blue D, Ceniza N, Mattson J C, Crisan D

Abstract excerpt

BACKGROUND: Several genetic defects are associated with increased risk of venous thrombosis. The factor V Leiden (FVL) and prothrombin G20210A mutations are the most frequent causes of inherited thrombophilia. OBJECTIVES: To evaluate combined genotyping for these 2 mutations in patients presenting with thromboembolic episodes and to correlate genotypic findings with clinical characteristics. RESULTS: Blood...

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Source

Identifiers

PMID: 11151062
DOI: 10.5858/2001-125-0105-CFVLAP

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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