Association of combined GIF290T>C heterozygous mutation/FUT2 secretor variant with neural tube defects.

about

Association of combined GIF290T>C heterozygous mutation/FUT2 secretor variant with neural tube defects.

Item

http://www.wikidata.org/entity/Q52564746

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Association of combined GIF290 ...... iant with neural tube defects.

@en

Association of combined GIF290 ...... iant with neural tube defects.

@nl

type

Item

label

Association of combined GIF290 ...... iant with neural tube defects.

@en

Association of combined GIF290 ...... iant with neural tube defects.

@nl

prefLabel

Association of combined GIF290 ...... iant with neural tube defects.

@en

Association of combined GIF290 ...... iant with neural tube defects.

@nl

P1476

Association of combined GIF290 ...... iant with neural tube defects.

@en

P2093

B Foliguet

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

B-M Caillierez-Fofou

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

C Chery

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

D Tramoy

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

F Feillet

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

J Voirin

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

J-L Guéant

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

R M Guéant-Rodriguez

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

T Josse

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

P2860

A genetic polymorphism in the coding region of the gastric intrinsic factor gene (GIF) is associated with congenital intrinsic factor deficiency

Folate deficiency and folic acid supplementation: the prevention of neural-tube defects and congenital heart defects

Malformations of the cranium, vertebral column, and related central nervous system: morphologic heterogeneity may indicate biological diversity.

Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome?

Common variants of FUT2 are associated with plasma vitamin B12 levels.

Vitamin B-12 and neural tube defects: the Canadian experience.

Folate and fetal programming: a play in epigenomics?

Prevalence of vitamin B-12 insufficiency during pregnancy and its effect on offspring birth weight: a systematic review and meta-analysis.

Cubilin, a high affinity receptor for fibroblast growth factor 8, is required for cell survival in the developing vertebrate head.

Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variant.

P304

191-193

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

P31

scholarly article

P356

10.1111/CGE.13104

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

P433

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

P478

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

P577

2017-07-25T00:00:00Z

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

P698

28742214

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