(Q46663105)

English

No association between common polymorphisms in genes of folate and homocysteine metabolism and the risk of Down's syndrome among French mothers

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

No association between common polymorphisms in genes of folate and homocysteine metabolism and the risk of Down's syndrome among French mothers (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

1 reference

based on heuristic

inferred from title

author name string

Abalo Chango

1

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

Nathalie Fillon-Emery

2

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

Clotilde Mircher

3

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

Henri Bléhaut

4

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

Daniel Lambert

5

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

Bernard Herbeth

6

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

S Jill James

7

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

Marie-Odile Réthoré

8

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

Jean Pierre Nicolas

9

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

publication date

1 August 2005

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

British Journal of Nutrition

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

94

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

2

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

166-169

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

MTRR and MTHFR polymorphism: link to Down syndrome?

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

Chromosomal control of meiotic cell division.

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

Methylenetetrahydrofolate reductase polymorphism in the etiology of Down syndrome

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

Methionine synthase (MTR) 2756 (A --> G) polymorphism, double heterozygosity methionine synthase 2756 AG/methionine synthase reductase (MTRR) 66 AG, and elevated homocysteinemia are three risk factors for having a child with Down syndrome

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

Frequency of Down's syndrome and neural-tube defects in the same family

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect.

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome?

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

Evaluation of genetic variants in the reduced folate carrier and in glutamate carboxypeptidase II for spina bifida risk

1 reference

https://api.crossref.org/works/10.1079%2FBJN20051490

21 January 2018

Identifiers

10.1079/BJN20051490

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/16115349

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q46663105&oldid=2125106442"