1. Expression profiles of the internal jugular and saphenous veins: Focus on hemostasis genes
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2. The present and future of whole-exome sequencing in studying and treating human reproductive disorders
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3. A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle
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4. IRX1 hypermethylation promotes heart failure by inhibiting CXCL14 expression
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5. Genomics and Epigenomics of Congenital Heart Defects: Expert Review and Lessons Learned in Africa
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6. ISL1 loss-of-function mutation contributes to congenital heart defects
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7. In Silico Analysis of Differential Gene Expression in Three Common Rat Models of Diastolic Dysfunction
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8. Application of next-generation sequencing for the diagnosis of fetuses with congenital heart defects
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9. Homeobox Genes and Homeodomain Proteins: New Insights into Cardiac Development, Degeneration and Regeneration
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