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Article

Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.

American journal of reproductive immunology (New York, N.Y. : 1989) - 1 May 2006

Coulam Carolyn B, Jeyendran Rajasinqam S, Fishel Laurence A, Roussev Roumen

Abstract excerpt

PROBLEM: Recurrent miscarriage is a heterogeneous condition. While the role of acquired thrombophilia has been accepted as an etiology of recurrent miscarriage, the contribution of specific inherited thrombophilic genes to this disorder has remained controversial. We compared the prevalence of 10...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 16635210
DOI: 10.1111/j.1600-0897.2006.00376.x

Genes

MTHFR

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16635210-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

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Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.PMID 16635210Read ↗

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A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.Semantic proximity Read ↗

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

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Fibrinolytic Defects and Recurrent MiscarriageSemantic proximity Read ↗

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