Discover Community Create You

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

[The role of 1691G>A (Leiden) mutation in Factor V gene, 20210G>A in prothrombin gene and 677C>T in MTHFR gene in etiology of early pregnancy loss].

Ginekologia polska - 1 Jun 2011

Slezak Ryszard, Łaczmański Łukasz, Karpiński Paweł, Reszczyńska-Slezak Dorota

Abstract excerpt

OBJECTIVES: The objective of this study was to investigate the prevalence of common hereditary risk factors for thrombophilia (mutations 1691G>A, 20210G>A and 677C>T variant in factor V Leiden (FV), prothrombin (FII) and MTHFR gene, respectively)--in a cohort of women with early pregnancy loss. MATERIAL AND METHODS: Frequency of mutations in FV, FII and MTHFR was assessed by PCR-RFLP or minisequencing in a cohort...

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 Factor V

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Methylenetetrahydrofolate Reductase (NADPH2)

Share to Point Mutation

Share to Pregnancy Trimester, First

Share to Prothrombin

Share to Reference Values

Share to Thrombophilia

Source

Identifiers

PMID: 21853935

Genes

MTHFR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[The role of 1691G>A (Leiden) mutation in Factor V gene, 20210G>A in prothrombin gene and 677C>T in MTHFR gene in etiology of early pregnancy loss].PMID 21853935Read ↗

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

Risk Factors of Thrombophilia-Related Mutations for Early and Late Pregnancy Loss.Semantic proximity Read ↗

[The 20210G>A and 19911A>G polymorphisms of prothrombin gene and recurrent miscarriages].Semantic proximity Read ↗

[Prevalence of factor V Leiden, hyperhomocysteinemia, prothrombin G20210A, and methylene tetrahydrofolate reductase C677T mutations in obstetrical complications].Semantic proximity Read ↗

Prevalence of F5 1691G>A, F2 20210G>A, and MTHFR 677C>T polymorphisms in Bosnian women with pregnancy loss.Semantic proximity Read ↗

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

Which thrombophilic gene mutations are risk factors for recurrent pregnancy loss?Semantic proximity Read ↗

Polymorphisms of ACE and thrombophilic genes: risk for recurrent pregnancy loss.Semantic proximity Read ↗

Thrombophilic polymorphisms are common in women with fetal loss without apparent cause.Semantic proximity Read ↗

Prothrombin G20210A mutation is associated with recurrent pregnancy loss: a systematic review and meta-analysis update.Semantic proximity Read ↗

[Factor V Leiden, FII G20210A, MTHFR C677T mutations as risk factors for venous thrombosis during pregnancy and puerperium].Semantic proximity Read ↗

Contribution of inherited thrombophilia to recurrent miscarriage in the Polish population.Semantic proximity Read ↗

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