Screening for new MTHFR polymorphisms and NTD risk (Q57677557)

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6 January 2020

title

Screening for new MTHFR polymorphisms and NTD risk (English)

1 reference

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6 January 2020

1

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6 January 2020

James L. Mills

2

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6 January 2020

Anne M. Molloy

5

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6 January 2020

Mary Conley

8

2 references

https://www.researchgate.net/scientific-contributions/39347795_Mary_Conley

29 April 2020

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6 January 2020

author name string

Anne Parle-McDermott

3

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6 January 2020

Faith Pangilinan

4

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6 January 2020

Christopher Cox

6

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6 January 2020

Andrea Weiler

7

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6 January 2020

Peadar N Kirke

9

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6 January 2020

John M Scott

10

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6 January 2020

Lawrence C Brody

11

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6 January 2020

Birth Defects Research Group

12

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6 January 2020

language of work or name

English

0 references

publication date

1 October 2005

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American Journal of Medical Genetics

6 January 2020

published in

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6 January 2020

volume

138A

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6 January 2020

issue

2

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6 January 2020

page(s)

99-106

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

6 January 2020

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FAJMG.A.30846

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

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FAJMG.A.30846

Loss of heterozygosity at the 5,10-methylenetetrahydrofolate reductase locus in human ovarian carcinomas

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FAJMG.A.30846

21 January 2018

Identifiers

DOI

10.1002/AJMG.A.30846

1 reference

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6 January 2020

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