MTHFR A1298C polymorphisms reduce the risk of congenital heart defects: a meta-analysis from 16 case-control studies.

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MTHFR A1298C polymorphisms reduce the risk of congenital heart defects: a meta-analysis from 16 case-control studies.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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MTHFR A1298C polymorphisms red ...... from 16 case-control studies.

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MTHFR A1298C polymorphisms red ...... from 16 case-control studies.

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MTHFR A1298C polymorphisms red ...... from 16 case-control studies.

@en

MTHFR A1298C polymorphisms red ...... from 16 case-control studies.

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MTHFR A1298C polymorphisms red ...... from 16 case-control studies.

@en

MTHFR A1298C polymorphisms red ...... from 16 case-control studies.

@nl

P1476

MTHFR A1298C polymorphisms red ...... from 16 case-control studies.

@en

P2093

Di Yu

http://www.w3.org/2001/XMLSchema#string

Xiaodong Zang

http://www.w3.org/2001/XMLSchema#string

Xuming Mo

http://www.w3.org/2001/XMLSchema#string

Zhongyuan Wen

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Zhulun Zhuang

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P275

Creative Commons Attribution 4.0 International

P2860

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.

Maternal folic acid supplementation and the risk of congenital heart defects in offspring: a meta-analysis of epidemiological observational studies.

Association between MTHFR polymorphisms and congenital heart disease: a meta-analysis based on 9,329 cases and 15,076 controls.

Maternal intake of fat, riboflavin and nicotinamide and the risk of having offspring with congenital heart defects.

Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome.

Homocysteine, folate, and congenital heart defects.

Mortality resulting from congenital heart disease among children and adults in the United States, 1999 to 2006

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases.

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congenital heart disease

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