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Journal Abstract Search

132 related items for PubMed ID: 18362318

  • 1. DLX3 mutation in a new family and its phenotypic variations.
    Lee SK, Lee ZH, Lee SJ, Ahn BD, Kim YJ, Lee SH, Kim JW.
    J Dent Res; 2008 Apr; 87(4):354-7. PubMed ID: 18362318
    [Abstract] [Full Text] [Related]

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  • 3. DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome.
    Wright JT, Hong SP, Simmons D, Daly B, Uebelhart D, Luder HU.
    Am J Med Genet A; 2008 Feb 01; 146A(3):343-9. PubMed ID: 18203197
    [Abstract] [Full Text] [Related]

  • 4. Severely hypoplastic amelogenesis imperfecta with taurodontism.
    Pavlic A, Lukinmaa PL, Nieminen P, Kiukkonen A, Alaluusua S.
    Int J Paediatr Dent; 2007 Jul 01; 17(4):259-66. PubMed ID: 17559453
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  • 6. Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho-dento-osseous syndrome.
    Whitehouse LLE, Smith CEL, Poulter JA, Brown CJ, Patel A, Lamb T, Brown LR, O'Sullivan EA, Mitchell RE, Berry IR, Charlton R, Inglehearn CF, Mighell AJ.
    Oral Dis; 2019 Jan 01; 25(1):182-191. PubMed ID: 30095208
    [Abstract] [Full Text] [Related]

  • 7. Unexpected identification of a recurrent mutation in the DLX3 gene causing amelogenesis imperfecta.
    Kim YJ, Seymen F, Koruyucu M, Kasimoglu Y, Gencay K, Shin TJ, Hyun HK, Lee ZH, Kim JW.
    Oral Dis; 2016 May 01; 22(4):297-302. PubMed ID: 26762616
    [Abstract] [Full Text] [Related]

  • 8. Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.
    Li Y, Han D, Zhang H, Liu H, Wong S, Zhao N, Qiu L, Feng H.
    Eur J Oral Sci; 2015 Aug 01; 123(4):228-34. PubMed ID: 26104267
    [Abstract] [Full Text] [Related]

  • 9. DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes.
    Nieminen P, Lukinmaa PL, Alapulli H, Methuen M, Suojärvi T, Kivirikko S, Peltola J, Asikainen M, Alaluusua S.
    Cells Tissues Organs; 2011 Aug 01; 194(1):49-59. PubMed ID: 21252474
    [Abstract] [Full Text] [Related]

  • 10. Craniofacial variations in the tricho-dento-osseous syndrome.
    Nguyen T, Phillips C, Frazier-Bower S, Wright T.
    Clin Genet; 2013 Apr 01; 83(4):375-9. PubMed ID: 22671030
    [Abstract] [Full Text] [Related]

  • 11. Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome.
    Price JA, Bowden DW, Wright JT, Pettenati MJ, Hart TC.
    Hum Mol Genet; 1998 Mar 01; 7(3):563-9. PubMed ID: 9467018
    [Abstract] [Full Text] [Related]

  • 12. Uncombable hair and atopic dermatitis in a case of trichodento-osseous syndrome.
    Mayer DE, Baal C, Litschauer-Poursadrollah M, Hemmer W, Jarisch R.
    J Dtsch Dermatol Ges; 2010 Feb 01; 8(2):102-4. PubMed ID: 20151948
    [Abstract] [Full Text] [Related]

  • 13. Clinical features of tricho-dento-osseous syndrome and presentation of three new cases: an addition to clinical heterogeneity.
    Islam M, Lurie AG, Reichenberger E.
    Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2005 Dec 01; 100(6):736-42. PubMed ID: 16301156
    [Abstract] [Full Text] [Related]

  • 14. Transcriptional factor DLX3 promotes the gene expression of enamel matrix proteins during amelogenesis.
    Zhang Z, Tian H, Lv P, Wang W, Jia Z, Wang S, Zhou C, Gao X.
    PLoS One; 2015 Dec 01; 10(3):e0121288. PubMed ID: 25815730
    [Abstract] [Full Text] [Related]

  • 15. Increased bone density associated with DLX3 mutation in the tricho-dento-osseous syndrome.
    Haldeman RJ, Cooper LF, Hart TC, Phillips C, Boyd C, Lester GE, Wright JT.
    Bone; 2004 Oct 01; 35(4):988-97. PubMed ID: 15454107
    [Abstract] [Full Text] [Related]

  • 16. Candidate gene strategy reveals ENAM mutations.
    Kang HY, Seymen F, Lee SK, Yildirim M, Tuna EB, Patir A, Lee KE, Kim JW.
    J Dent Res; 2009 Mar 01; 88(3):266-9. PubMed ID: 19329462
    [Abstract] [Full Text] [Related]

  • 17. Novel DLX3 variant identified in a family with tricho-dento-osseous syndrome.
    Liu H, Wang Y, Liu H, Yu M, Zheng J, Feng H, Liu Y, Han D.
    Arch Oral Biol; 2022 Sep 01; 141():105479. PubMed ID: 35714441
    [Abstract] [Full Text] [Related]

  • 18. Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.
    Zhao N, Han D, Liu H, Li Y, Wong SW, Cao Z, Xu J, Zhang X, Cai T, Wang Y, Feng H.
    Sci Rep; 2016 Dec 07; 6():38680. PubMed ID: 27924851
    [Abstract] [Full Text] [Related]

  • 19. Trichodentoosseous (TDO) syndrome: case report and literature review.
    Seow WK.
    Pediatr Dent; 1993 Dec 07; 15(5):355-61. PubMed ID: 8302675
    [Abstract] [Full Text] [Related]

  • 20. A common DLX3 gene mutation is responsible for tricho-dento-osseous syndrome in Virginia and North Carolina families.
    Price JA, Wright JT, Kula K, Bowden DW, Hart TC.
    J Med Genet; 1998 Oct 07; 35(10):825-8. PubMed ID: 9783705
    [Abstract] [Full Text] [Related]

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