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Journal Abstract Search

226 related items for PubMed ID: 23718693

  • 21. Nonsyndromic oligodontia : Does the Tooth Agenesis Code (TAC) enable prediction of the causative mutation?
    Bock NC, Lenz S, Ruiz-Heiland G, Ruf S.
    J Orofac Orthop; 2017 Mar; 78(2):112-120. PubMed ID: 28204848
    [Abstract] [Full Text] [Related]

  • 22. Genes affecting tooth morphogenesis.
    Kapadia H, Mues G, D'Souza R.
    Orthod Craniofac Res; 2007 Aug; 10(3):105-13. PubMed ID: 17651126
    [Abstract] [Full Text] [Related]

  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25. 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 30; 123(1):1-8. PubMed ID: 25545742
    [Abstract] [Full Text] [Related]

  • 26. Oral clefts and syndromic forms of tooth agenesis as models for genetics of isolated tooth agenesis.
    Vieira AR.
    J Dent Res; 2003 Mar 30; 82(3):162-5. PubMed ID: 12598542
    [Abstract] [Full Text] [Related]

  • 27. 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 30; 16(6):1112-6. PubMed ID: 24103583
    [Abstract] [Full Text] [Related]

  • 28. Association of MSX1 with nonsyndromic cleft lip and palate in a Colombian population.
    Otero L, Gutiérrez S, Cháves M, Vargas C, Bérmudez L.
    Cleft Palate Craniofac J; 2007 Nov 30; 44(6):653-6. PubMed ID: 18177186
    [Abstract] [Full Text] [Related]

  • 29. [Msh homebox-1 polymorphisms and susceptibility to 198 sporadic tooth agenesis: a case-control study].
    Wang H, Wang L, Pan YC, Ma JQ, Zhang WB.
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2010 Mar 30; 45(3):135-40. PubMed ID: 20450679
    [Abstract] [Full Text] [Related]

  • 30. MSH homeobox 1 polymorphisms and the risk of non-syndromic orofacial clefts: a meta-analysis.
    Gu M, Zhang Y, Liu H, Liu J, Zhu D, Yang X.
    Eur J Oral Sci; 2018 Jun 30; 126(3):180-185. PubMed ID: 29664137
    [Abstract] [Full Text] [Related]

  • 31. MSX1 gene polymorphisms in non-syndromic cleft lip and/or palate.
    Cardoso ML, Bezerra JF, Oliveira GH, Soares CD, Oliveira SR, de Souza KS, da Silva HP, Silbiger VN, Luchessi AD, Fajardo CM, Hirata RD, Almeida MG, Hirata MH, Rezende AA.
    Oral Dis; 2013 Jul 30; 19(5):507-12. PubMed ID: 23130753
    [Abstract] [Full Text] [Related]

  • 32. 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
    [Abstract] [Full Text] [Related]

  • 33. Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region.
    Slayton RL, Williams L, Murray JC, Wheeler JJ, Lidral AC, Nishimura CJ.
    Cleft Palate Craniofac J; 2003 May 30; 40(3):274-9. PubMed ID: 12733956
    [Abstract] [Full Text] [Related]

  • 34. 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
    [Abstract] [Full Text] [Related]

  • 35. Gene-gene interaction between MSX1 and TP63 in Asian case-parent trios with nonsyndromic cleft lip with or without cleft palate.
    Liu D, Schwender H, Wang M, Wang H, Wang P, Zhu H, Zhou Z, Li J, Wu T, Beaty TH.
    Birth Defects Res; 2018 Mar 01; 110(4):317-324. PubMed ID: 29341488
    [Abstract] [Full Text] [Related]

  • 36. 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 01; 93(5):452-8. PubMed ID: 24554542
    [Abstract] [Full Text] [Related]

  • 37. Association between MSX1 variants and oral clefts in Han Chinese in western China.
    Huang YQ, Ma J, Ma M, Deng Y, Li YD, Ren HW, Zhao GZ, Guo SS, Wang YY, Zhang GX, Shi B.
    DNA Cell Biol; 2011 Dec 01; 30(12):1057-61. PubMed ID: 21689018
    [Abstract] [Full Text] [Related]

  • 38. Sequence analysis of PAX9, MSX1 and AXIN2 genes in a Chinese oligodontia family.
    Wang J, Jian F, Chen J, Wang H, Lin Y, Yang Z, Pan X, Lai W.
    Arch Oral Biol; 2011 Oct 01; 56(10):1027-34. PubMed ID: 21530942
    [Abstract] [Full Text] [Related]

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