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Journal Abstract Search

112 related items for PubMed ID: 24935264

  • 1. Novel complex disease allele mutations in cleidocranial dysplasia patients.
    Anthonappa RP, Yan-Hui F, King NM, Rabie AB, You-Qiang S.
    J Oral Pathol Med; 2014 Nov; 43(10):798-800. PubMed ID: 24935264
    [Abstract] [Full Text] [Related]

  • 2. Novel RUNX2 mutations in Chinese individuals with cleidocranial dysplasia.
    Zhang CY, Zheng SG, Wang YX, Zhu JX, Zhu X, Zhao YM, Ge LH.
    J Dent Res; 2009 Sep; 88(9):861-6. PubMed ID: 19767586
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  • 6. Cleidocranial dysplasia: oral features and genetic analysis of 11 patients.
    Bufalino A, Paranaíba LM, Gouvêa AF, Gueiros LA, Martelli-Júnior H, Junior JJ, Lopes MA, Graner E, De Almeida OP, Vargas PA, Coletta RD.
    Oral Dis; 2012 Mar; 18(2):184-90. PubMed ID: 22023169
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  • 7. RUNX2 mutations in cleidocranial dysplasia patients.
    Ryoo HM, Kang HY, Lee SK, Lee KE, Kim JW.
    Oral Dis; 2010 Jan; 16(1):55-60. PubMed ID: 19744171
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  • 8. A novel gene mutation of Runx2 in cleidocranial dysplasia.
    Peng YJ, Chen QY, Fu DJ, Liu ZM, Mao TT, Li J, She WT.
    J Huazhong Univ Sci Technolog Med Sci; 2017 Oct; 37(5):772-776. PubMed ID: 29058294
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  • 11. A new phenotypic variant in cleidocranial dysplasia (CCD) associated with mutation c.391C>T of the RUNX2 gene.
    Callea M, Fattori F, Yavuz I, Bertini E.
    BMJ Case Rep; 2012 Dec 05; 2012():. PubMed ID: 23220435
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  • 13. A novel RUNX2 mutation (T420I) in Chinese patients with cleidocranial dysplasia.
    Wang GX, Sun RP, Song FL.
    Genet Mol Res; 2010 Jan 12; 9(1):41-7. PubMed ID: 20082269
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  • 14. RUNX2 mutations in cleidocranial dysplasia.
    Lee KE, Seymen F, Ko J, Yildirim M, Tuna EB, Gencay K, Kim JW.
    Genet Mol Res; 2013 Oct 15; 12(4):4567-74. PubMed ID: 24222232
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  • 15. A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia.
    Xu W, Chen Q, Liu C, Chen J, Xiong F, Wu B.
    BMC Med Genet; 2017 Feb 07; 18(1):13. PubMed ID: 28173761
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  • 16. Dental Follicle Cells Participate in Tooth Eruption via the RUNX2-MiR-31-SATB2 Loop.
    Ge J, Guo S, Fu Y, Zhou P, Zhang P, Du Y, Li M, Cheng J, Jiang H.
    J Dent Res; 2015 Jul 07; 94(7):936-44. PubMed ID: 25818585
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  • 18. [Gene mutation detection in a cleidocranial dysplasia family].
    Wang Y, Wu H, Zhang XX, Zhao HS, Feng HL.
    Zhonghua Kou Qiang Yi Xue Za Zhi; 2005 Nov 07; 40(6):459-62. PubMed ID: 16329826
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  • 19. A novel RUNX2 missense mutation predicted to disrupt DNA binding causes cleidocranial dysplasia in a large Chinese family with hyperplastic nails.
    Tang S, Xu Q, Xu X, Du J, Yang X, Jiang Y, Wang X, Speck N, Huang T.
    BMC Med Genet; 2007 Dec 31; 8():82. PubMed ID: 18166138
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