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Journal Abstract Search

262 related items for PubMed ID: 21040462

  • 1. Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia.
    Suda N, Hattori M, Kosaki K, Banshodani A, Kozai K, Tanimoto K, Moriyama K.
    Orthod Craniofac Res; 2010 Nov; 13(4):197-202. PubMed ID: 21040462
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  • 4. 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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  • 5. Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations.
    Cunningham ML, Seto ML, Hing AV, Bull MJ, Hopkin RJ, Leppig KA.
    Birth Defects Res A Clin Mol Teratol; 2006 Feb; 76(2):78-85. PubMed ID: 16463420
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  • 6. 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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  • 7. Delayed tooth eruption and suppressed osteoclast number in the eruption pathway of heterozygous Runx2/Cbfa1 knockout mice.
    Yoda S, Suda N, Kitahara Y, Komori T, Ohyama K.
    Arch Oral Biol; 2004 Jun; 49(6):435-42. PubMed ID: 15099800
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  • 13. Clinical spectrum of cleidocranial dysplasia in a family with twins.
    Wang J, Huang X, Lai C, Jiang K.
    Pediatr Int; 2013 Jun; 55(3):392-5. PubMed ID: 23782374
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  • 14. [Orthodontic and oral surgery therapy in cleidocranial dysplasia].
    Balaton G, Tarján I, Balaton P, Barabási Z, Gyulai Gál S, Nagy K, Vajó Z.
    Fogorv Sz; 2007 Feb; 100(1):17-21. PubMed ID: 17444132
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  • 16. 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
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  • 17. Cleidocranial dysplasia: a family report.
    Chelvan HT, Malathi N, Kailasam V, Ponnudurai A.
    J Indian Soc Pedod Prev Dent; 2009 Nov; 27(4):249-52. PubMed ID: 19915277
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