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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

233 related items for PubMed ID: 21591244

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  • 23. TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy.
    Cabuk F, Karabulut HG, Tuncali T, Karademir S, Bozdayi M, Tükün A.
    Turk J Pediatr; 2007; 49(1):61-8. PubMed ID: 17479646
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  • 24. Cardiac malformations and alteration of TGFbeta signaling system in diabetic embryopathy.
    Zhao Z.
    Birth Defects Res B Dev Reprod Toxicol; 2010 Apr; 89(2):97-105. PubMed ID: 20127828
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  • 25. Second lineage of heart forming region provides new understanding of conotruncal heart defects.
    Nakajima Y.
    Congenit Anom (Kyoto); 2010 Mar; 50(1):8-14. PubMed ID: 20050864
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  • 28. Conotruncal defects associated with anomalous pulmonary venous connections.
    Bajolle F, Zaffran S, Losay J, Ou P, Buckingham M, Bonnet D.
    Arch Cardiovasc Dis; 2009 Feb; 102(2):105-10. PubMed ID: 19303577
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  • 33. The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis.
    Kelly RG, Jerome-Majewska LA, Papaioannou VE.
    Hum Mol Genet; 2004 Nov 15; 13(22):2829-40. PubMed ID: 15385444
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  • 34. The pattern of the coronary arterial orifices in hearts with congenital malformations of the outflow tracts: a marker of rotation of the outflow tract during cardiac development?
    Houyel L, Bajolle F, Capderou A, Laux D, Parisot P, Bonnet D.
    J Anat; 2013 Mar 15; 222(3):349-57. PubMed ID: 23317176
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  • 35. Cardiac neural crest expression of Hand2 regulates outflow and second heart field development.
    Morikawa Y, Cserjesi P.
    Circ Res; 2008 Dec 05; 103(12):1422-9. PubMed ID: 19008477
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  • 36. Lack of Gata3 results in conotruncal heart anomalies in mouse.
    Raid R, Krinka D, Bakhoff L, Abdelwahid E, Jokinen E, Kärner M, Malva M, Meier R, Pelliniemi LJ, Ploom M, Sizarov A, Pooga M, Karis A.
    Mech Dev; 2009 Dec 05; 126(1-2):80-9. PubMed ID: 18955134
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  • 40. Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis.
    Morishima M, Yanagisawa H, Yanagisawa M, Baldini A.
    Dev Dyn; 2003 Sep 05; 228(1):95-104. PubMed ID: 12950083
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