Associations between two genetic variants in NKX2-5 and risk of congenital heart disease in Chinese population: a meta-analysis
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PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger SyndromeGerbode Ventricular Septal Defect -A Rare Cardiac Anomaly Associated with Genetic Variants in Indian Population- A Case Series.Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population.Associations of NKX2-5 Genetic Polymorphisms with the Risk of Congenital Heart Disease: A Meta-analysis.
P2860
Associations between two genetic variants in NKX2-5 and risk of congenital heart disease in Chinese population: a meta-analysis
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2013 nî lūn-bûn
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2013 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2013年の論文
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2013年論文
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2013年論文
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2013年論文
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2013年論文
@zh-mo
2013年論文
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2013年论文
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Associations between two genet ...... se population: a meta-analysis
@ast
Associations between two genet ...... se population: a meta-analysis
@en
Associations between two genet ...... se population: a meta-analysis
@nl
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label
Associations between two genet ...... se population: a meta-analysis
@ast
Associations between two genet ...... se population: a meta-analysis
@en
Associations between two genet ...... se population: a meta-analysis
@nl
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Associations between two genet ...... se population: a meta-analysis
@ast
Associations between two genet ...... se population: a meta-analysis
@en
Associations between two genet ...... se population: a meta-analysis
@nl
P2093
P2860
P1433
P1476
Associations between two genet ...... se population: a meta-analysis
@en
P2093
Beibei Zhu
Ranran Song
Rong Zhong
Xiao-Ping Miao
Zhenling Wang
P2860
P304
P356
10.1371/JOURNAL.PONE.0070979
P407
P577
2013-08-02T00:00:00Z