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Article

Thrombophilic genes alterations as risk factor for recurrent pregnancy loss.

The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians - 1 Jan 2016

Farahmand Kamelia, Totonchi Mehdi, Hashemi Mehrdad, Reyhani Sabet Fakhreddin, Kalantari Hamid, Gourabi Hamid, Mohseni Meybodi Anahita

Abstract excerpt

OBJECTIVE: The important polymorphisms leading to inherited thrombophilia are Factor V Leiden (FVL), Prothrombin G20210A and MTHFR C677T and A1298C. The frequencies also the correlation among these polymorphisms and RPL have been reported controversially in various populations. Our clinic is one of the referral centers in reproductive biomedicine in which patients in all over Iran refer to; thus the results of...

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Source

Identifiers

PMID: 26135458
DOI: 10.3109/14767058.2015.1044431

Genes

MTHFR

Variants

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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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