These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

404 related items for PubMed ID: 25860641

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. TBX20 loss-of-function mutation contributes to double outlet right ventricle.
    Pan Y, Geng R, Zhou N, Zheng GF, Zhao H, Wang J, Zhao CM, Qiu XB, Yang YQ, Liu XY.
    Int J Mol Med; 2015 Apr; 35(4):1058-66. PubMed ID: 25625280
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. 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; 33(5):1201-8. PubMed ID: 24604414
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block.
    Zhang Y, Sun YM, Xu YJ, Zhao CM, Yuan F, Guo XJ, Guo YH, Yang CX, Gu JN, Qiao Q, Wang J, Yang YQ.
    Int Heart J; 2020 Jul 30; 61(4):761-768. PubMed ID: 32641638
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. 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 Jul 30; 14(11):1143-1153. PubMed ID: 29104469
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.
    Huang RT, Wang J, Xue S, Qiu XB, Shi HY, Li RG, Qu XK, Yang XX, Liu H, Li N, Li YJ, Xu YJ, Yang YQ.
    Int J Med Sci; 2017 Jul 30; 14(4):323-332. PubMed ID: 28553164
    [Abstract] [Full Text] [Related]

  • 13. A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle.
    Lu CX, Wang W, Wang Q, Liu XY, Yang YQ.
    Pediatr Cardiol; 2018 Apr 30; 39(4):794-804. PubMed ID: 29468350
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. PITX2 loss-of-function mutation contributes to tetralogy of Fallot.
    Sun YM, Wang J, Qiu XB, Yuan F, Xu YJ, Li RG, Qu XK, Huang RT, Xue S, Yang YQ.
    Gene; 2016 Feb 15; 577(2):258-64. PubMed ID: 26657035
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 21.