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30 results on '"Xing Yuan Liu"'

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1. Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease

2. SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial Hypertension

3. GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve

4. A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect

5. GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve

6. MEF2C loss-of-function mutation contributes to congenital heart defects

7. MESP1 loss-of-function mutation contributes to double outlet right ventricle

8. HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle

9. Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation

10. A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot

11. TBX20 loss-of-function mutation contributes to double outlet right ventricle

12. A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve

13. A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle

14. Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease

15. Novel GATA4 mutations in patients with congenital ventricular septal defects

16. PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome

17. A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease

18. A novel NKX2.6 mutation associated with congenital ventricular septal defect

19. GATA5 loss-of-function mutations underlie tetralogy of fallot

20. GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect

21. A novel GATA6 mutation associated with congenital ventricular septal defect

22. A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect

23. A novel GATA4 mutation responsible for congenital ventricular septal defects

24. Involvement of a novel GATA4 mutation in atrial septal defects

25. A novel NKX2-5 mutation in familial ventricular septal defect

26. Novel NKX2-5 mutations in patients with familial atrial septal defects

27. A novel GATA6 mutation in patients with tetralogy of Fallot or atrial septal defect

28. MESP1 loss‑of‑function mutation contributes to double outlet right ventricle.

29. Novel NKX2-5 Mutations in Patients With Familial Atrial Septal Defects.

30. A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve.

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