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Journal Abstract Search

282 related items for PubMed ID: 23828301

  • 1. Genetic background of nonsyndromic oligodontia: a systematic review and meta-analysis.
    Ruf S, Klimas D, Hönemann M, Jabir S.
    J Orofac Orthop; 2013 Jul; 74(4):295-308. PubMed ID: 23828301
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  • 7. Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis.
    Yu M, Wong SW, Han D, Cai T.
    Oral Dis; 2019 Apr; 25(3):646-651. PubMed ID: 29969831
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  • 8. Clinical and genetic evaluation of a Chinese family with isolated oligodontia.
    Qin H, Xu HZ, Xuan K.
    Arch Oral Biol; 2013 Sep; 58(9):1180-6. PubMed ID: 23731659
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  • 9. Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families.
    Mu YD, Xu Z, Contreras CI, McDaniel JS, Donly KJ, Chen S.
    Genet Mol Res; 2013 Oct 10; 12(4):4446-58. PubMed ID: 24222224
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  • 10. Axis inhibition protein 2 polymorphisms may be a risk factor for families with isolated oligodontia.
    Qin H, Cai J.
    Mol Med Rep; 2015 Mar 10; 11(3):1899-904. PubMed ID: 25377791
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  • 11. Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia.
    Wong S, Liu H, Bai B, Chang H, Zhao H, Wang Y, Han D, Feng H.
    Arch Oral Biol; 2014 Mar 10; 59(3):349-53. PubMed ID: 24581859
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  • 12. Mutations in MSX1, PAX9 and MMP20 genes in Saudi Arabian patients with tooth agenesis.
    Shahid M, Balto HA, Al-Hammad N, Joshi S, Khalil HS, Somily AM, Sinjilawi NA, Al-Ghamdi S, Faiyaz-Ul-Haque M, Dhillon VS.
    Eur J Med Genet; 2016 Aug 10; 59(8):377-85. PubMed ID: 27365112
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  • 13. Familial oligodontia and regional odontodysplasia associated with a PAX9 initiation codon mutation.
    Koskinen S, Keski-Filppula R, Alapulli H, Nieminen P, Anttonen V.
    Clin Oral Investig; 2019 Nov 10; 23(11):4107-4111. PubMed ID: 30809714
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  • 14. Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis.
    Callahan N, Modesto A, Meira R, Seymen F, Patir A, Vieira AR.
    Arch Oral Biol; 2009 Jan 10; 54(1):45-9. PubMed ID: 18790474
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  • 15. Targeted next-generation sequencing (NGS) analysis of mutations in nonsyndromic tooth agenesis candidate genes : Analysis of a Turkish cohort.
    Keskin G, Karaer K, Uçar Gündoğar Z.
    J Orofac Orthop; 2022 Oct 10; 83(Suppl 1):65-74. PubMed ID: 33725141
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  • 16. Investigating the etiology of multiple tooth agenesis in three sisters with severe oligodontia.
    Swinnen S, Bailleul-Forestier I, Arte S, Nieminen P, Devriendt K, Carels C.
    Orthod Craniofac Res; 2008 Feb 10; 11(1):24-31. PubMed ID: 18199077
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  • 17. A novel initiation codon mutation of PAX9 in a family with oligodontia.
    Liang J, Qin C, Yue H, He H, Bian Z.
    Arch Oral Biol; 2016 Jan 10; 61():144-8. PubMed ID: 26571067
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  • 18. PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China.
    Wang J, Xu Y, Chen J, Wang F, Huang R, Wu S, Shu L, Qiu J, Yang Z, Xue J, Wang R, Zhao J, Lai W.
    J Appl Oral Sci; 2013 Jan 10; 21(3):256-64. PubMed ID: 23857653
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  • 19. Novel nonsense mutation in MSX1 in familial nonsyndromic oligodontia: subcellular localization and role of homeodomain/MH4.
    Kimura M, Machida J, Yamaguchi S, Shibata A, Tatematsu T, Miyachi H, Jezewski PA, Nakayama A, Higashi Y, Shimozato K, Tokita Y.
    Eur J Oral Sci; 2014 Feb 10; 122(1):15-20. PubMed ID: 24329876
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  • 20. Associations between the risk of tooth agenesis and single-nucleotide polymorphisms of MSX1 and PAX9 genes in nonsyndromic cleft patients.
    Seo YJ, Park JW, Kim YH, Baek SH.
    Angle Orthod; 2013 Nov 10; 83(6):1036-42. PubMed ID: 23718693
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