(Q44509442)

3 December 2017

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

1 reference

3 December 2017

1 reference

1 reference

7

Rima Rozen

1 reference

3 December 2017

Isabelle Morin

1

1 reference

3 December 2017

Angela M Devlin

2

1 reference

3 December 2017

Daniel Leclerc

3

1 reference

3 December 2017

Nelly Sabbaghian

4

1 reference

3 December 2017

Charles H Halsted

5

1 reference

3 December 2017

Richard Finnell

6

1 reference

3 December 2017

1 July 2003

1 reference

Molecular Genetics and Metabolism

3 December 2017

1 reference

3 December 2017

79

1 reference

3 December 2017

3

1 reference

3 December 2017

197-200

1 reference

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

3 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900086-6

7 January 2021

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900086-6

7 January 2021

Glutamate carboxypeptidase II: a polymorphism associated with lower levels of serum folate and hyperhomocysteinemia.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900086-6

7 January 2021

Studies with His475Tyr glutamate carboxipeptidase II polymorphism and neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900086-6

7 January 2021

A polymorphism (80G->A) in the reduced folate carrier gene and its associations with folate status and homocysteinemia

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900086-6

7 January 2021

Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900086-6

7 January 2021

Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900086-6

7 January 2021

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/10.1016%2FS1096-7192%2803%2900086-6

7 January 2021

Folate levels and neural tube defects. Implications for prevention

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900086-6

7 January 2021

10.1016/S1096-7192(03)00086-6

Identifiers

DOI

1 reference

3 December 2017

1 reference