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Keyword [conotruncal heart defects]
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1. The Genetic Study Of Conotruncal Heart Defects
2. Research On 22q11.2 Microdeletion In Patients With Cono-truncal Deformanity
3. Methylenetetrahydrofolate Reductase C677T And Reduced Folate Carrier80G>A Polymorphisms And Conotruncal Heart Defects Effects Of Mitochondrial Aldehyde Dehydrogenase-2Genotype On Cardioprotection In Conotruncal Heart Defect Patients Undergoing Open-hea
4. Frequency Of Chromosome 22q11.2 Microdeletion In Sporadic Non-syndromic Conotruncal Heart Defects By Multiplex Ligation-dependent Probe Amplification
5. Impact Of Syndrome And CNVs On The Outcome Of Surgery Of Conotruncal Heart Defects
6. Mutation Screening And Pathogenesis Exploration Among Susceptibility Genes Of Conotruncal Heart Defects
7. Study On The Pathogenic Mechanisms Of Polymorphisms In 3'UTR Of NOTCH1,NOTCH2 And JAG1 Genes In Conotruncal Heart Defects
8. Identification Of TBX2 And TBX3 Variants In Conotruncal Heart Defect Patients And Study Of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect
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