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Article

Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss.

Human reproduction (Oxford, England) - 1 Jun 2002

Carp Howard, Salomon Ophira, Seidman Daniel, Dardik Rima, Rosenberg Nurith, Inbal Aida

Abstract excerpt

BACKGROUND: The genetic predispositions to venous thrombosis such as factor V Leiden (FVL) mutation (Arg 506 Gln), prothrombin (FII) gene mutation (G20210A), and mutation of the methylenetetrahydrofolate reductase (MTHFR) gene (C677T) have been reported to be associated with recurrent pregnancy loss. This paper examines the prevalence of markers for genetic thrombophilias in women with recurrent miscarriage....

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

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Source

Identifiers

PMID: 12042290
DOI: 10.1093/humrep/17.6.1633

Genes

MTHFR

Variants

Provenance

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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Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss.PMID 12042290Read ↗

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Factor V Leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriagesSemantic proximity Read ↗

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Genetic thrombophilic mutations among couples with recurrent miscarriage.Semantic proximity Read ↗

[Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].Semantic proximity Read ↗

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