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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

246 related items for PubMed ID: 21519287

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  • 3. DNA methylation status of NKX2-5, GATA4 and HAND1 in patients with tetralogy of fallot.
    Sheng W, Qian Y, Wang H, Ma X, Zhang P, Diao L, An Q, Chen L, Ma D, Huang G.
    BMC Med Genomics; 2013 Nov 01; 6():46. PubMed ID: 24182332
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  • 4. Search of somatic GATA4 and NKX2.5 gene mutations in sporadic septal heart defects.
    Salazar M, Consoli F, Villegas V, Caicedo V, Maddaloni V, Daniele P, Caianiello G, Pachón S, Nuñez F, Limongelli G, Pacileo G, Marino B, Bernal JE, De Luca A, Dallapiccola B.
    Eur J Med Genet; 2011 Nov 01; 54(3):306-9. PubMed ID: 21276881
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  • 5. HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.
    Wang J, Hu XQ, Guo YH, Gu JY, Xu JH, Li YJ, Li N, Yang XX, Yang YQ.
    Pediatr Cardiol; 2017 Mar 01; 38(3):547-557. PubMed ID: 27942761
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  • 10. A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.
    Sun YM, Wang J, Qiu XB, Yuan F, Li RG, Xu YJ, Qu XK, Shi HY, Hou XM, Huang RT, Xue S, Yang YQ.
    G3 (Bethesda); 2016 Apr 07; 6(4):987-92. PubMed ID: 26865696
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  • 13. Search of Somatic Mutations of NKX2-5 and GATA4 Genes in Chinese Patients with Sporadic Congenital Heart Disease.
    Yin J, Qian J, Dai G, Wang C, Qin Y, Xu T, Li Z, Zhang H, Yang S.
    Pediatr Cardiol; 2019 Jan 07; 40(1):17-22. PubMed ID: 30121862
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  • 15. Nuclear Receptor-Like Structure and Interaction of Congenital Heart Disease-Associated Factors GATA4 and NKX2-5.
    Kinnunen S, Välimäki M, Tölli M, Wohlfahrt G, Darwich R, Komati H, Nemer M, Ruskoaho H.
    PLoS One; 2015 Jan 07; 10(12):e0144145. PubMed ID: 26642209
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  • 19. GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot.
    El Bouchikhi I, Belhassan K, Moufid FZ, Houssaini MI, Bouguenouch L, Samri I, Bouhrim M, Ouldim K, Atmani S.
    Afr Health Sci; 2018 Dec 07; 18(4):922-930. PubMed ID: 30766556
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  • 20. 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 Dec 07; 14(4):323-332. PubMed ID: 28553164
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