(Q74348099)

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The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations

scientific article published on 01 April 2000

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10 November 2019

The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations (English)

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10 November 2019

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I P Dávalos

1

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10 November 2019

N Olivares

2

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10 November 2019

M T Castillo

3

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10 November 2019

J M Cantú

4

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10 November 2019

B Ibarra

5

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10 November 2019

L Sandoval

6

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10 November 2019

M C Morán

7

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10 November 2019

M P Gallegos

8

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10 November 2019

R Chakraborty

9

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10 November 2019

F Rivas

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10 November 2019

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1 April 2000

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10 November 2019

Annales de Génétique

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10 November 2019

43

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10 November 2019

2

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10 November 2019

89-92

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10 November 2019

Prevalence of the mutation C677 --> T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Spina bifida, 677T-->C mutation, and role of folate

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Thermolabile methylenetetrahydrofolate reductase in patients with coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Increased risk of recurrence of pregnancies complicated by fetal neural tube defects in mothers receiving poor diets, and possible benefit of dietary counselling

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

High prevalence of the thermolabile methylenetetrahydrofolate reductase variant in Mexico: a country with a very high prevalence of neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Reproductive history in mothers of children with neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Worldwide distribution of a common methylenetetrahydrofolate reductase mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Possible prevention of neural-tube defects by periconceptional vitamin supplementation

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

The thermolabile variant of methylenetetrahydrofolate reductase (MTHFR) is not a major risk factor for neural tube defect in American Caucasians. The NTD Collaborative Group

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Maternal hyperhomocysteinemia: a risk factor for neural-tube defects?

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Is the common 677C-->T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0003-3995%2800%2990012-1

7 January 2021

Identifiers

10.1016/S0003-3995(00)90012-1

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998450%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10998450%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

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