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Journal Abstract Search

268 related items for PubMed ID: 22297032

  • 1. Novel MSX1 mutation in a family with autosomal-dominant hypodontia of second premolars and third molars.
    Mostowska A, Biedziak B, Jagodzinski PP.
    Arch Oral Biol; 2012 Jun; 57(6):790-5. PubMed ID: 22297032
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  • 2. A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.
    Abdalla EM, Mostowska A, Jagodziński PP, Dwidar K, Ismail SR.
    Arch Oral Biol; 2014 Jul; 59(7):722-8. PubMed ID: 24798981
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  • 3. 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; 115(4):330-3. PubMed ID: 17697174
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  • 5. A human MSX1 homeodomain missense mutation causes selective tooth agenesis.
    Vastardis H, Karimbux N, Guthua SW, Seidman JG, Seidman CE.
    Nat Genet; 1996 Aug; 13(4):417-21. PubMed ID: 8696335
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  • 8. Mutations in WNT10A are present in more than half of isolated hypodontia cases.
    van den Boogaard MJ, Créton M, Bronkhorst Y, van der Hout A, Hennekam E, Lindhout D, Cune M, Ploos van Amstel HK.
    J Med Genet; 2012 May; 49(5):327-31. PubMed ID: 22581971
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  • 9. Effects of PAX9 and MSX1 gene variants to hypodontia, tooth size and the type of congenitally missing teeth.
    Kirac D, Eraydin F, Avcilar T, Ulucan K, Özdemir F, Guney AI, Kaspar EÇ, Keshi E, Isbir T.
    Cell Mol Biol (Noisy-le-grand); 2016 Nov 30; 62(13):78-84. PubMed ID: 28040065
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  • 10. [Correlation between the phenotype and genotype of tooth agenesis patients by tooth agenesis code].
    Gong Y, Feng HL, He HY, Ge YJ.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2010 Jun 30; 32(3):254-9. PubMed ID: 20602873
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  • 11. Novel MSX1 frameshift causes autosomal-dominant oligodontia.
    Kim JW, Simmer JP, Lin BP, Hu JC.
    J Dent Res; 2006 Mar 30; 85(3):267-71. PubMed ID: 16498076
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  • 12. 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 30; 93(3):245-9. PubMed ID: 24436340
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  • 15. Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis.
    Pinho T, Silva-Fernandes A, Bousbaa H, Maciel P.
    Eur J Orthod; 2010 Oct 30; 32(5):582-8. PubMed ID: 20660504
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  • 20. Mutation analysis by direct and whole exome sequencing in familial and sporadic tooth agenesis.
    Salvi A, Giacopuzzi E, Bardellini E, Amadori F, Ferrari L, De Petro G, Borsani G, Majorana A.
    Int J Mol Med; 2016 Nov 30; 38(5):1338-1348. PubMed ID: 27665865
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