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Journal Abstract Search

262 related items for PubMed ID: 29104469

  • 1. MEF2C loss-of-function mutation contributes to congenital heart defects.
    Qiao XH, Wang F, Zhang XL, Huang RT, Xue S, Wang J, Qiu XB, Liu XY, Yang YQ.
    Int J Med Sci; 2017; 14(11):1143-1153. PubMed ID: 29104469
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  • 6. ISL1 loss-of-function mutation contributes to congenital heart defects.
    Ma L, Wang J, Li L, Qiao Q, Di RM, Li XM, Xu YJ, Zhang M, Li RG, Qiu XB, Li X, Yang YQ.
    Heart Vessels; 2019 Apr; 34(4):658-668. PubMed ID: 30390123
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  • 7. A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect.
    Qiao XH, Wang Q, Wang J, Liu XY, Xu YJ, Huang RT, Xue S, Li YJ, Zhang M, Qu XK, Li RG, Qiu XB, Yang YQ.
    Eur J Med Genet; 2018 Apr; 61(4):197-203. PubMed ID: 29222010
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  • 10. PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.
    Zhao CM, Peng LY, Li L, Liu XY, Wang J, Zhang XL, Yuan F, Li RG, Qiu XB, Yang YQ.
    PLoS One; 2015 Apr; 10(4):e0124409. PubMed ID: 25893250
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  • 11. A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle.
    Wang Z, Song HM, Wang F, Zhao CM, Huang RT, Xue S, Li RG, Qiu XB, Xu YJ, Liu XY, Yang YQ.
    Int Heart J; 2019 Sep 27; 60(5):1113-1122. PubMed ID: 31484864
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  • 17. A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect.
    Yang YQ, Li L, Wang J, Liu XY, Chen XZ, Zhang W, Wang XZ, Jiang JQ, Liu X, Fang WY.
    Pediatr Cardiol; 2012 Apr 27; 33(4):539-46. PubMed ID: 22101736
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  • 19. Novel PITX2c loss-of-function mutations associated with complex congenital heart disease.
    Wei D, Gong XH, Qiu G, Wang J, Yang YQ.
    Int J Mol Med; 2014 May 27; 33(5):1201-8. PubMed ID: 24604414
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  • 20. MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.
    Yuan F, Qiu ZH, Wang XH, Sun YM, Wang J, Li RG, Liu H, Zhang M, Shi HY, Zhao L, Jiang WF, Liu X, Qiu XB, Qu XK, Yang YQ.
    Clin Chem Lab Med; 2018 Feb 23; 56(3):502-511. PubMed ID: 28902616
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