(Q44038927)

29 November 2017

title

C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy (English)

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29 November 2017

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1

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29 November 2017

7

Giandomenico Palka

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29 November 2017

4

Ivana Antonucci

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29 November 2017

Valentina Gatta

2

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29 November 2017

Anna Rita Gaspari

series ordinal

3

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29 November 2017

Elisena Morizio

series ordinal

5

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29 November 2017

Giuseppe Calabrese

series ordinal

6

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29 November 2017

language of work or name

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1 June 2002

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European Journal of Human Genetics

29 November 2017

published in

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29 November 2017

volume

10

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29 November 2017

issue

6

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29 November 2017

page(s)

388-390

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Methionine metabolism in mammals

29 November 2017

cites work

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

Homozygous methylenetetrahydrofolate reductase C677T mutation and male infertility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

Maternal folate polymorphisms and the etiology of human nondisjunction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

The VITA project: C677T mutation in the methylene-tetrahydrofolate reductase gene and risk of venous thromboembolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

Methylenetetrahydrofolate reductase mutation and neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

Methylenetetrahydrofolate reductase and neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

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/10.1038%2FSJ.EJHG.5200819

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/10.1038%2FSJ.EJHG.5200819

7 January 2021

Heterozygote advantage of the MTHFR gene in patients with neural-tube defect and their relatives

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

7 January 2021

Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200819

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5200819

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Dimensions Publication ID

29 November 2017

1006582631

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1 reference