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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

188 related items for PubMed ID: 23713051

  • 21. Type-I umbilical-systemic shunt with abnormal connection to azygos vein in fetus with de-novo TBX5 mutation related to Holt-Oram syndrome.
    Achiron R, Har-Toov J, Kivilevitch Z.
    Ultrasound Obstet Gynecol; 2024 May; 63(5):709-711. PubMed ID: 38197531
    [No Abstract] [Full Text] [Related]

  • 22. Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease.
    Smemo S, Campos LC, Moskowitz IP, Krieger JE, Pereira AC, Nobrega MA.
    Hum Mol Genet; 2012 Jul 15; 21(14):3255-63. PubMed ID: 22543974
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  • 26. TBX5 variants and cardiac phenotype: A systematic review of the literature and a novel variant.
    Møller Nielsen AK, Dehn AM, Hjortdal V, Larsen LA.
    Eur J Med Genet; 2024 Apr 15; 68():104920. PubMed ID: 38336121
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  • 29. Genetic Analyses Identified a SALL4 Gene Mutation Associated with Holt-Oram Syndrome.
    Li B, Chen S, Sun K, Xu R, Wu Y.
    DNA Cell Biol; 2018 Apr 15; 37(4):398-404. PubMed ID: 29461882
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  • 30. Tbx5 inhibits hedgehog signaling in determination of digit identity.
    Xu H, Xiang M, Qin Y, Cheng H, Chen D, Fu Q, Zhang KK, Xie L.
    Hum Mol Genet; 2020 Jun 03; 29(9):1405-1416. PubMed ID: 31373354
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  • 35. Congenital heart diseases and their association with the variant distribution features on susceptibility genes.
    Su W, Zhu P, Wang R, Wu Q, Wang M, Zhang X, Mei L, Tang J, Kumar M, Wang X, Su L, Dong N.
    Clin Genet; 2017 Mar 03; 91(3):349-354. PubMed ID: 27426723
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  • 36. TBX5: A Key Regulator of Heart Development.
    Steimle JD, Moskowitz IP.
    Curr Top Dev Biol; 2017 Mar 03; 122():195-221. PubMed ID: 28057264
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  • 37. [Holt-Oram syndrome: study of 7 cases].
    Martínez-García M, Lorda-Sanchez I, García-Hoyos M, Ramos C, Ayuso C, Trujillo-Tiebas MJ.
    Med Clin (Barc); 2010 Nov 13; 135(14):653-7. PubMed ID: 21070912
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  • 38. Ulnar mammary syndrome.
    Ramirez RN, Kozin SH.
    J Hand Surg Am; 2014 Apr 13; 39(4):803-5. PubMed ID: 24679913
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  • 39. Prenatal diagnosis of complex phenotype in a 13-week-old fetus with an interstitial multigene deletion 20q13.13.-q13.2 by chromosomal microarray.
    Stipoljev F, Miric-Tesanic D, Hafner T, Barbalic M, Logara M, Lasan-Trcic R, Vicic A, Gjergja-Juraski R.
    Eur J Med Genet; 2017 Nov 13; 60(11):589-594. PubMed ID: 28807863
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