Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion.

Annals of hematology - 1 Apr 2006

Behjati Reza, Modarressi Mohammad Hossein, Jeddi-Tehrani Mahmood, Dokoohaki Pouneh, Ghasemi Jamileh, Zarnani Amir Hassan, Aarabi Mahmoud, Memariani Toktam, Ghaffari Marefat, Akhondi Mehdi A

Abstract excerpt

Factor V Leiden (FVL) G1691A, methylenetetrahydrofolate reductase (MTHFR) C677T, and factor II (FII) G20210A mutations are three important causes of thrombophilia, the condition that might be related to infertility and recurrent spontaneous abortion (RSA). In this study we evaluated the presence of these three mutations in 36 female patients with unexplained infertility, 65 female patients with unexplained RSA,...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Abortion, Habitual
Share to Comorbidity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Factor V

Share to Infertility

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Prothrombin

Share to Thrombophilia

Source

Identifiers

PMID: 16450127
DOI: 10.1007/s00277-005-0021-0

Genes

MTHFR
APC

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion.PMID 16450127Read ↗

Association between FVL G1691A, FII G20210A, and MTHFR C677T and A1298C polymorphisms and Turkish women with recurrent pregnancy loss.Semantic proximity Read ↗

Association between thrombophilia gene polymorphisms and recurrent pregnancy loss risk in the Iranian populationSemantic proximity Read ↗

Genetics of suspected thrombophilia in Serbian females with infertility, including three cases, homozygous for FII 20210A or FV 1691A mutations.Semantic proximity Read ↗

Factor V Leiden and prothrombin gene mutations in Egyptian cases with unexplained recurrent pregnancy loss.Semantic proximity Read ↗

Thrombophilic genes alterations as risk factor for recurrent pregnancy loss.Semantic proximity Read ↗

[Inherited thrombophilic factors in women with secondary infertility].Semantic proximity Read ↗

The association between thrombophilic genes alterations and poor ovarian response in infertile women: a retrospective case-control study.Semantic proximity Read ↗

Which are the most common thrombophilic genetic nucleotide polymorphisms in infertile women undergoing an IVF cycle?Semantic proximity Read ↗

Polymorphisms of plasminogen activator inhibitor-1, angiotensin converting enzyme and coagulation factor XIII genes in patients with recurrent spontaneous abortion.Semantic proximity Read ↗

Factor V leiden and factor II G20210A mutations in patients with recurrent abortion.Semantic proximity Read ↗

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

Inherited thrombophilia and anticoagulant therapy for women with reproductive failureSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.