(Q77220767)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10190487%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

title

Decreased proportion of female newborn infants homozygous for the 677 C-->T mutation in methylenetetrahydrofolate reductase (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10190487%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

author name string

R Rozen

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10190487%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

F C Fraser

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10190487%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

G Shaw

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10190487%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

publication date

1 March 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10190487%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part A

3 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10190487%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

volume

83

1 reference

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3 December 2019

issue

2

1 reference

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3 December 2019

page(s)

142-143

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10190487%20AND%20SRC:MED&resulttype=core&format=json

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

3 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990312%2983%3A2%3C142%3A%3AAID-AJMG12%3E3.0.CO%3B2-Y

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990312%2983%3A2%3C142%3A%3AAID-AJMG12%3E3.0.CO%3B2-Y

Genetic selection and folate intake during pregnancy

21 January 2018

1 reference

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Genetic risk factor for unexplained recurrent early pregnancy loss

21 January 2018

1 reference

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Isolated oral cleft malformations: associations with maternal and infant characteristics in a California population

21 January 2018

1 reference

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Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990312%2983%3A2%3C142%3A%3AAID-AJMG12%3E3.0.CO%3B2-Y

Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990312%2983%3A2%3C142%3A%3AAID-AJMG12%3E3.0.CO%3B2-Y

Is the common 677C-->T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990312%2983%3A2%3C142%3A%3AAID-AJMG12%3E3.0.CO%3B2-Y

Heterozygote advantage of the MTHFR gene in patients with neural-tube defect and their relatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819990312%2983%3A2%3C142%3A%3AAID-AJMG12%3E3.0.CO%3B2-Y

10.1002/(SICI)1096-8628(19990312)83:2<142::AID-AJMG12>3.0.CO;2-Y

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10190487%20AND%20SRC:MED&resulttype=core&format=json

3 December 2019

1 reference