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Journal Abstract Search

411 related items for PubMed ID: 27054699

  • 21.
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  • 22. A novel EDAR missense mutation identified by whole-exome sequencing with non-syndromic tooth agenesis in a Chinese family.
    Zhang H, Kong X, Ren J, Yuan S, Liu C, Hou Y, Liu Y, Meng L, Zhang G, Du Q, Shen W.
    Mol Genet Genomic Med; 2021 Jun; 9(6):e1684. PubMed ID: 33943035
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  • 23. 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 Jun; 21(3):256-64. PubMed ID: 23857653
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  • 25. Novel mutations identified in patients with tooth agenesis by whole-exome sequencing.
    Zhao K, Lian M, Zou D, Huang W, Zhou W, Shen Y, Wang F, Wu Y.
    Oral Dis; 2019 Mar; 25(2):523-534. PubMed ID: 30417976
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  • 26. Novel PAX9 mutation associated with syndromic tooth agenesis.
    Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP.
    Eur J Oral Sci; 2013 Oct; 121(5):403-11. PubMed ID: 24028587
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  • 27. 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; 38(5):1338-1348. PubMed ID: 27665865
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  • 28.
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  • 29. Non-syndromic tooth agenesis associated with a nonsense mutation in ectodysplasin-A (EDA).
    Nikopensius T, Annilo T, Jagomägi T, Gilissen C, Kals M, Krjutškov K, Mägi R, Eelmets M, Gerst-Talas U, Remm M, Saag M, Hoischen A, Metspalu A.
    J Dent Res; 2013 Jun; 92(6):507-11. PubMed ID: 23603338
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  • 31. Oligodontia and curly hair occur with ectodysplasin-a mutations.
    Lee KE, Ko J, Shin TJ, Hyun HK, Lee SH, Kim JW.
    J Dent Res; 2014 Apr; 93(4):371-5. PubMed ID: 24487376
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  • 32. Identification of a novel mutation of the EDA gene in X-linked hypohidrotic ectodermal dysplasia.
    Xue JJ, Tan B, Gao QP, Zhu GS, Liang DS, Wu LQ.
    Genet Mol Res; 2015 Dec 02; 14(4):15779-82. PubMed ID: 26634545
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  • 33. A novel frameshift mutation in the EDA gene in an Iranian patient affected by X-linked hypohidrotic ectodermal dysplasia.
    Rahbaran M, Hassani Doabsari M, Salavitabar S, Mokhberian N, Morovvati Z, Morovvati S.
    Cell Mol Biol Lett; 2019 Dec 02; 24():54. PubMed ID: 31452656
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  • 37. 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 02; 78(2):112-120. PubMed ID: 28204848
    [Abstract] [Full Text] [Related]

  • 38. KDF1 is a novel candidate gene of non-syndromic tooth agenesis.
    Zeng B, Lu H, Xiao X, Yu X, Li S, Zhu L, Yu D, Zhao W.
    Arch Oral Biol; 2019 Jan 02; 97():131-136. PubMed ID: 30384154
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