(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

default for all languages

No label defined

No description defined

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"