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Journal Abstract Search

157 related items for PubMed ID: 14517948

  • 1. Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot.
    Pizzuti A, Sarkozy A, Newton AL, Conti E, Flex E, Digilio MC, Amati F, Gianni D, Tandoi C, Marino B, Crossley M, Dallapiccola B.
    Hum Mutat; 2003 Nov; 22(5):372-7. PubMed ID: 14517948
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  • 2. New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle.
    De Luca A, Sarkozy A, Ferese R, Consoli F, Lepri F, Dentici ML, Vergara P, De Zorzi A, Versacci P, Digilio MC, Marino B, Dallapiccola B.
    Clin Genet; 2011 Aug; 80(2):184-90. PubMed ID: 20807224
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  • 3. Identification of novel significant variants of ZFPM2/FOG2 in non-syndromic Tetralogy of Fallot and double outlet right ventricle in a Chinese Han population.
    Huang X, Niu W, Zhang Z, Zhou C, Xu Z, Liu J, Su Z, Ding W, Zhang H.
    Mol Biol Rep; 2014 Aug; 41(4):2671-7. PubMed ID: 24469719
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  • 4. Novel missense variants of ZFPM2/FOG2 identified in conotruncal heart defect patients do not impair interaction with GATA4.
    Zhang W, Shen L, Deng Z, Ding Y, Mo X, Xu Z, Gao Q, Yi L.
    PLoS One; 2014 Aug; 9(7):e102379. PubMed ID: 25025186
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  • 7. Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.
    Qian Y, Xiao D, Guo X, Chen H, Hao L, Ma X, Huang G, Ma D, Wang H.
    J Transl Med; 2017 Apr 03; 15(1):69. PubMed ID: 28372585
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  • 8. GATA4 loss-of-function mutations underlie familial tetralogy of fallot.
    Yang YQ, Gharibeh L, Li RG, Xin YF, Wang J, Liu ZM, Qiu XB, Xu YJ, Xu L, Qu XK, Liu X, Fang WY, Huang RT, Xue S, Nemer G.
    Hum Mutat; 2013 Dec 03; 34(12):1662-71. PubMed ID: 24000169
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  • 11. Mutations in the FOG2/ZFPM2 gene are associated with anomalies of human testis determination.
    Bashamboo A, Brauner R, Bignon-Topalovic J, Lortat-Jacob S, Karageorgou V, Lourenco D, Guffanti A, McElreavey K.
    Hum Mol Genet; 2014 Jul 15; 23(14):3657-65. PubMed ID: 24549039
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  • 13. Target Sequencing Identifies a Novel Mutation of ZFPM2 in a Chinese Newborn with Tetralogy of Fallot.
    Zhu L, Yue JW, Yang XH.
    Ann Clin Lab Sci; 2019 Mar 15; 49(2):274-275. PubMed ID: 31028076
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  • 14. Genetic screening of the canine zinc finger protein multitype 2 (cZFPM2) gene in dogs with tetralogy of Fallot (TOF).
    Lee JS, Hyun C.
    J Anim Breed Genet; 2009 Aug 15; 126(4):304-10. PubMed ID: 19630881
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  • 18. Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects.
    Hamanoue H, Rahayuningsih SE, Hirahara Y, Itoh J, Yokoyama U, Mizuguchi T, Saitsu H, Miyake N, Hirahara F, Matsumoto N.
    Cardiol Young; 2009 Sep 15; 19(5):482-5. PubMed ID: 19678963
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  • 19. ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresia.
    Sarkozy A, Conti E, D'Agostino R, Digilio MC, Formigari R, Picchio F, Marino B, Pizzuti A, Dallapiccola B.
    Am J Med Genet A; 2005 Feb 15; 133A(1):68-70. PubMed ID: 15643620
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  • 20. 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
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