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Journal Abstract Search

277 related items for PubMed ID: 22171628

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  • 3. Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.
    Paulussen AD, Steyls A, Vanoevelen J, van Tienen FH, Krapels IP, Claes GR, Chocron S, Velter C, Tan-Sindhunata GM, Lundin C, Valenzuela I, Nagy B, Bache I, Maroun LL, Avela K, Brunner HG, Smeets HJ, Bakkers J, van den Wijngaard A.
    Eur J Hum Genet; 2016 Dec; 24(12):1783-1791. PubMed ID: 27406248
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  • 5. ZIC3 in Heterotaxy.
    Bellchambers HM, Ware SM.
    Adv Exp Med Biol; 2018 Dec; 1046():301-327. PubMed ID: 29442328
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  • 9. A mouse model of conduction system patterning abnormalities in heterotaxy syndrome.
    Czosek RJ, Haaning A, Ware SM.
    Pediatr Res; 2010 Oct; 68(4):275-80. PubMed ID: 20581739
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  • 12. The phenotypic spectrum of ZIC3 mutations includes isolated d-transposition of the great arteries and double outlet right ventricle.
    D'Alessandro LC, Latney BC, Paluru PC, Goldmuntz E.
    Am J Med Genet A; 2013 Apr; 161A(4):792-802. PubMed ID: 23427188
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  • 15. Craniorachischisis and heterotaxia with heart disease in twins: link or change nature?
    Bianca S, Bartoloni G, Barone C, Barrano B, Boemi G, De Filippo V, Indaco L, Cataliotti A, Ettore G.
    Congenit Heart Dis; 2010 Apr; 5(5):450-3. PubMed ID: 21087431
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  • 16. Hydrops fetalis in PKD1L1-related heterotaxy: Report of two foetuses and expanding the phenotypic and molecular spectrum.
    Correa ARE, Endrakanti M, Naini K, Kabra M, Gupta N.
    Ann Hum Genet; 2021 May; 85(3-4):138-145. PubMed ID: 33655537
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  • 17. A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect.
    Wang Y, Dai X, Liu H, Peng J, Chen J.
    Prenat Diagn; 2023 Mar; 43(3):275-279. PubMed ID: 36567274
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  • 19. Dextrocardia and asplenia in situs inversus totalis in a baby: a case report.
    Kumar A, Singh MK, Yadav N.
    J Med Case Rep; 2014 Dec 05; 8():408. PubMed ID: 25477011
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  • 20. X-linked situs abnormalities result from mutations in ZIC3.
    Gebbia M, Ferrero GB, Pilia G, Bassi MT, Aylsworth A, Penman-Splitt M, Bird LM, Bamforth JS, Burn J, Schlessinger D, Nelson DL, Casey B.
    Nat Genet; 1997 Nov 05; 17(3):305-8. PubMed ID: 9354794
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