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Journal Abstract Search

209 related items for PubMed ID: 20660504

  • 1.
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  • 2. WNT10A coding variants and maxillary lateral incisor agenesis with associated dental anomalies.
    Mostowska A, Biedziak B, Zadurska M, Matuszewska-Trojan S, Jagodziński PP.
    Eur J Oral Sci; 2015 Feb; 123(1):1-8. PubMed ID: 25545742
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  • 3. Identification of genetic risk factors for maxillary lateral incisor agenesis.
    Alves-Ferreira M, Pinho T, Sousa A, Sequeiros J, Lemos C, Alonso I.
    J Dent Res; 2014 May; 93(5):452-8. PubMed ID: 24554542
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  • 4. 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; 59(8):377-85. PubMed ID: 27365112
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  • 5. PAX9 and MSX1 transcription factor genes in non-syndromic dental agenesis.
    Paixão-Côrtes VR, Braga T, Salzano FM, Mundstock K, Mundstock CA, Bortolini MC.
    Arch Oral Biol; 2011 Apr; 56(4):337-44. PubMed ID: 21111400
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  • 8. [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; 32(3):254-9. PubMed ID: 20602873
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  • 9. Maxillary canine anomalies and tooth agenesis.
    Camilleri S.
    Eur J Orthod; 2005 Oct; 27(5):450-6. PubMed ID: 16093260
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  • 10. Concomitant occurrence of canine malposition and tooth agenesis: evidence of orofacial genetic fields.
    Peck S, Peck L, Kataja M.
    Am J Orthod Dentofacial Orthop; 2002 Dec; 122(6):657-60. PubMed ID: 12490878
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  • 11. 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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  • 14. 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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  • 15. Genes affecting tooth morphogenesis.
    Kapadia H, Mues G, D'Souza R.
    Orthod Craniofac Res; 2007 Nov; 10(4):237-44. PubMed ID: 17973693
    [Abstract] [Full Text] [Related]

  • 16. 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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  • 18. Novel MSX1 frameshift causes autosomal-dominant oligodontia.
    Kim JW, Simmer JP, Lin BP, Hu JC.
    J Dent Res; 2006 Mar; 85(3):267-71. PubMed ID: 16498076
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  • 19. MSX1 and PAX9 investigation in monozygotic twins with variable expression of tooth agenesis.
    Lopez SI, Mundstock KS, Paixão-Côrtes VR, Schüler-Faccini L, Mundstock CA, Bortolini MC, Salzano FM.
    Twin Res Hum Genet; 2013 Dec; 16(6):1112-6. PubMed ID: 24103583
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  • 20. Familial aggregation of maxillary lateral incisor agenesis.
    Pinho T, Maciel P, Lemos C, Sousa A.
    J Dent Res; 2010 Jun; 89(6):621-5. PubMed ID: 20400722
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