A Targeted, Next-Generation Genetic Sequencing Study on Tetralogy of Fallot, Combined With Cleft Lip and Palate

about

A Targeted, Next-Generation Genetic Sequencing Study on Tetralogy of Fallot, Combined With Cleft Lip and Palate

Item

http://www.wikidata.org/entity/Q42009370

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

A Targeted, Next-Generation Ge ...... ined With Cleft Lip and Palate

@en

A Targeted, Next-Generation Ge ...... ined With Cleft Lip and Palate

@nl

type

Item

label

A Targeted, Next-Generation Ge ...... ined With Cleft Lip and Palate

@en

A Targeted, Next-Generation Ge ...... ined With Cleft Lip and Palate

@nl

prefLabel

A Targeted, Next-Generation Ge ...... ined With Cleft Lip and Palate

@en

A Targeted, Next-Generation Ge ...... ined With Cleft Lip and Palate

@nl

P1476

A Targeted, Next-Generation Ge ...... ined With Cleft Lip and Palate

@en

P2093

Fei Zhang

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

Haisong Bu

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

Lin Liu

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

Shijun Hu

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

Tianli Zhao

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

Yifeng Yang

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

Zhiping Tan

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

P2860

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate

Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition.

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death.

Familial Tetralogy of Fallot caused by mutation in the jagged1 gene.

Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot.

Association between 5, 10-methylenetetrahydrofolate reductase (MTHFR) polymorphisms and congenital heart disease: A meta-analysis

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

P304

e351-e355

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

P31

scholarly article

P356

10.1097/SCS.0000000000003598

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

P433

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

P478

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

P577

2017-02-22T00:00:00Z

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

P698

28230599

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

P932

5459582

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