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Journal Abstract Search

180 related items for PubMed ID: 16479262

  • 1.
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  • 2. A novel mutation in PAX9 causes familial form of molar oligodontia.
    Mostowska A, Biedziak B, Trzeciak WH.
    Eur J Hum Genet; 2006 Feb; 14(2):173-9. PubMed ID: 16333316
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  • 3. [Functional analysis of novel mutations in PAX9 associated with familial oligodontia].
    Zhao JL, Chen YX, Bao L, Wu TJ, Zhou L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug; 22(4):419-22. PubMed ID: 16086281
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  • 7. Genes affecting tooth morphogenesis.
    Kapadia H, Mues G, D'Souza R.
    Orthod Craniofac Res; 2007 Nov; 10(4):237-44. PubMed ID: 17973693
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  • 8. Genes affecting tooth morphogenesis.
    Kapadia H, Mues G, D'Souza R.
    Orthod Craniofac Res; 2007 Aug; 10(3):105-13. PubMed ID: 17651126
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  • 9. Novel PAX9 mutations cause non-syndromic tooth agenesis.
    Mitsui SN, Yasue A, Masuda K, Watanabe K, Horiuchi S, Imoto I, Tanaka E.
    J Dent Res; 2014 Mar; 93(3):245-9. PubMed ID: 24436340
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  • 10. Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.
    Nieminen P, Arte S, Tanner D, Paulin L, Alaluusua S, Thesleff I, Pirinen S.
    Eur J Hum Genet; 2001 Oct; 9(10):743-6. PubMed ID: 11781684
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  • 11. Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9.
    Wang Y, Groppe JC, Wu J, Ogawa T, Mues G, D'Souza RN, Kapadia H.
    Hum Mol Genet; 2009 Aug 01; 18(15):2863-74. PubMed ID: 19429910
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  • 12. A novel mutation in human PAX9 causes molar oligodontia.
    Frazier-Bowers SA, Guo DC, Cavender A, Xue L, Evans B, King T, Milewicz D, D'Souza RN.
    J Dent Res; 2002 Feb 01; 81(2):129-33. PubMed ID: 11827258
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  • 13. A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth.
    Hansen L, Kreiborg S, Jarlov H, Niebuhr E, Eiberg H.
    Eur J Oral Sci; 2007 Aug 01; 115(4):330-3. PubMed ID: 17697174
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  • 14. Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype.
    Wong SW, Han D, Zhang H, Liu Y, Zhang X, Miao MZ, Wang Y, Zhao N, Zeng L, Bai B, Wang YX, Liu H, Frazier-Bowers SA, Feng H.
    J Dent Res; 2018 Feb 01; 97(2):155-162. PubMed ID: 28910570
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  • 15. Novel missense mutation in PAX9 gene associated with familial tooth agenesis.
    Boeira BR, Echeverrigaray S.
    J Oral Pathol Med; 2013 Jan 01; 42(1):99-105. PubMed ID: 22747565
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  • 16. A novel missense mutation in the paired domain of human PAX9 causes oligodontia.
    Zhao J, Hu Q, Chen Y, Luo S, Bao L, Xu Y.
    Am J Med Genet A; 2007 Nov 01; 143A(21):2592-7. PubMed ID: 17910065
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  • 17. A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia.
    Jumlongras D, Lin JY, Chapra A, Seidman CE, Seidman JG, Maas RL, Olsen BR.
    Hum Genet; 2004 Feb 01; 114(3):242-9. PubMed ID: 14689302
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  • 18. Characterization of PAX9 variant P20L identified in a Japanese family with tooth agenesis.
    Murakami A, Yasuhira S, Mayama H, Miura H, Maesawa C, Satoh K.
    PLoS One; 2017 Feb 01; 12(10):e0186260. PubMed ID: 29023497
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  • 19. Identification of a novel mutation in the PAX9 gene in a family affected by oligodontia and other dental anomalies.
    Tallón-Walton V, Manzanares-Céspedes MC, Arte S, Carvalho-Lobato P, Valdivia-Gandur I, Garcia-Susperregui A, Ventura F, Nieminen P.
    Eur J Oral Sci; 2007 Dec 01; 115(6):427-32. PubMed ID: 18028048
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  • 20. Novel PAX9 mutation associated with syndromic tooth agenesis.
    Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP.
    Eur J Oral Sci; 2013 Oct 01; 121(5):403-11. PubMed ID: 24028587
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