Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population.

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Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population.

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2018 nî lūn-bûn

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2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

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2018年學術文章

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name

Association of NRG1 and AUTS2 ...... in a South Chinese population.

@en

Association of NRG1 and AUTS2 ...... in a South Chinese population.

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Item

label

Association of NRG1 and AUTS2 ...... in a South Chinese population.

@en

Association of NRG1 and AUTS2 ...... in a South Chinese population.

@nl

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Association of NRG1 and AUTS2 ...... in a South Chinese population.

@en

Association of NRG1 and AUTS2 ...... in a South Chinese population.

@nl

P1476

Association of NRG1 and AUTS2 ...... in a South Chinese population

@en

P2093

Deli Zhu

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Jixiao Zeng

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

Qiang Wu

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

Ruizhong Zhang

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Xiaoli Xie

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Yan Zhang

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P2860

PLINK: a tool set for whole-genome association and population-based linkage analyses

Contribution of rare and common variants determine complex diseases-Hirschsprung disease as a model

Haploview: analysis and visualization of LD and haplotype maps

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

A new multipoint method for genome-wide association studies by imputation of genotypes

COXPRESdb in 2015: coexpression database for animal species by DNA-microarray and RNAseq-based expression data with multiple quality assessment systems.

Comprehensive analysis of RET common and rare variants in a series of Spanish Hirschsprung patients confirms a synergistic effect of both kinds of events.

Association study of neuregulin-1 gene polymorphisms in a North Indian schizophrenia sample.

Toxicity from radiation therapy associated with abnormal transcriptional responses to DNA damage

Differential contributions of rare and common, coding and noncoding Ret mutations to multifactorial Hirschsprung disease liability

P304

2190-2199

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scholarly article

P356

10.1111/JCMM.13498

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P433

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P478

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P50

Hai-ming Xia

P577

2018-01-29T00:00:00Z

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P698

29377512

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5867083

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