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Article

Aetiology of pre-eclampsia and thrombophilic genetic mutations.

Clinical science (London, England : 1979) - 1 Sept 2003

Hayashi Masatoshi

Abstract excerpt

Schlembach and co-workers in this issue of Clinical Science have studied the association of maternal and/or fetal factor V Leiden (FVL) and prothrombin G20210A gene mutation with HELLP syndrome and intrauterine growth restriction (IUGR) to confirm whether these genetic mutations are important risk factors for the pathogenesis of the HELLP syndrome, leading to an inadequate maternal-fetal circulation. Results...

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Identifiers

PMID: 12780341
DOI: 10.1042/CS20030181

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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.

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