(Q51777758)

12 April 2018

title

MTRR 66A>G polymorphism in relation to congenital heart defects. (English)

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author

Henk J Blom

7

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author name string

Ingrid M van Beynum

1

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Margreet Kouwenberg

2

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Livia Kapusta

3

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Martin den Heijer

4

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Ivon J M van der Linden

5

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Otto Daniels

6

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publication date

1 January 2006

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Clinical Chemistry and Laboratory Medicine

published in

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volume

44

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issue

11

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page(s)

1317-1323

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The incidence of congenital heart disease

cites work

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2006.254

A simple salting out procedure for extracting DNA from human nucleated cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2006.254

Genetic determinants of plasma total homocysteine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2006.254

Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2006.254

Differences in the efficiency of reductive activation of methionine synthase and exogenous electron acceptors between the common polymorphic variants of human methionine synthase reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2006.254

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2006.254

Congenital heart defects and genetic variants in the methylenetetrahydroflate reductase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2006.254

21 January 2018

Identifiers

DOI

10.1515/CCLM.2006.254

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12 April 2018