Evaluation of chromosomal abnormalities and common trombophilic mutations in cases with recurrent miscarriage (Q35665231)

9 August 2017

title

Evaluation of chromosomal abnormalities and common trombophilic mutations in cases with recurrent miscarriage (English)

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9 August 2017

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Ahmet Karatas

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9 August 2017

Recep Eroz

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9 August 2017

Mustafa Albayrak

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9 August 2017

Tulay Ozlu

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9 August 2017

Bulent Cakmak

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9 August 2017

Fatih Keskin

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9 August 2017

language of work or name

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1 March 2014

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9 August 2017

published in

African Health Sciences

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9 August 2017

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9 August 2017

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9 August 2017

page(s)

216-222

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Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Genetics of pregnancy loss

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Evaluation of the association between hereditary thrombophilias and recurrent pregnancy loss: a meta-analysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Thrombophilic disorders and fetal loss: a meta-analysis

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Clinical and laboratory management of the prothrombin G20210A mutation

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Clinical utility of factor V leiden (R506Q) testing for the diagnosis and management of thromboembolic disorders

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Genetic factors in recurrent pregnancy loss

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Maternal age and fetal loss: population based register linkage study

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Hemostasis during pregnancy and puerperium

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

12 July 2018

1 reference

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A cytogenetic study of repeated spontaneous abortions.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Relationship between Y-chromosome length and first-trimester spontaneous abortions.

12 July 2018

1 reference

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Cytogenetic analysis of 750 spontaneous abortions with the direct-preparation method of chorionic villi and its implications for studying genetic causes of pregnancy wastage

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Cytogenetic studies in couples experiencing repeated pregnancy losses

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss

12 July 2018

1 reference

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MTHFR C677T and factor V Leiden in recurrent pregnancy loss: a study among an endogamous group in North India

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Association of parental hyperhomocysteinemia and C677T Methylene tetrahydrofolate reductase (MTHFR) polymorphism with recurrent pregnancy loss

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

ACE and MTHFR gene polymorphisms in unexplained recurrent pregnancy loss

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Relationship between methylenetetrahydrofolate reductase polymorphism and homocysteine levels in women with recurrent pregnancy loss: a nutrigenetic perspective

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Recurrent abortions in Asian Indians: no role of factor V Leiden Hong Kong/Cambridge mutation and MTHFR polymorphism.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Chromosomal studies in infertile men with oligozoospermia & non-obstructive azoospermia.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

Factor V Leiden and acquired activated protein C resistance among 1000 women with recurrent miscarriage.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449075

High prevalence of a mutation in the factor V gene within the U.K. population: relationship to activated protein C resistance and familial thrombosis.

25 September 2018

1 reference

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Obesity increases the risk of spontaneous abortion during infertility treatment

25 September 2018

1 reference

12 December 2020

The clinical use of karyotyping spontaneous abortions

1 reference

12 December 2020

Poor obstetric outcome in subsequent pregnancies in women with prior fetal death

1 reference

12 December 2020

Fetal loss after implantation. A prospective study

1 reference

12 December 2020

Haemostasis in normal pregnancy

1 reference

12 December 2020

Recurrent miscarriage

1 reference

12 December 2020

An informative protocol for the investigation of recurrent miscarriage: preliminary experience of 500 consecutive cases

1 reference

12 December 2020

Factor V Leiden is associated with repeated and recurrent unexplained fetal losses

1 reference

12 December 2020

Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia

1 reference

12 December 2020

Geographic distribution of the 20210 G to A prothrombin variant

1 reference

12 December 2020

Thrombophilic polymorphisms are common in women with fetal loss without apparent cause

1 reference

12 December 2020

Recurrent miscarriage

1 reference

12 December 2020

Identifiers

DOI

10.4314/AHS.V14I1.34

1 reference

release_2hvnylzjsbcinihzdnoisfscfa

9 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2hvnylzjsbcinihzdnoisfscfa

24 November 2022

mapped directly with Wikidata item

PMC publication ID

4449075

1 reference

9 August 2017

1 reference