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Journal Abstract Search

197 related items for PubMed ID: 24966961

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  • 2. A novel single-base deletion mutation of the RUNX2 gene in a Chinese family with cleidocranial dysplasia.
    Fang CY, Xue JJ, Tan L, Jiang CH, Gao QP, Liang DS, Wu LQ.
    Genet Mol Res; 2011 Dec 14; 10(4):3539-44. PubMed ID: 22194205
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  • 7. Mutations in the RUNX2 gene in Chinese patients with cleidocranial dysplasia.
    Xuan D, Li S, Zhang X, Hu F, Lin L, Wang C, Zhang J.
    Ann Clin Lab Sci; 2008 Dec 14; 38(1):15-24. PubMed ID: 18316777
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  • 8. RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
    Li Y, Pan W, Xu W, He N, Chen X, Liu H, Darryl Quarles L, Zhou H, Xiao Z.
    Mutagenesis; 2009 Sep 14; 24(5):425-31. PubMed ID: 19515746
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  • 9. Familial cleidocranial dysplasia misdiagnosed as rickets over three generations.
    Franceschi R, Maines E, Fedrizzi M, Piemontese MR, De Bonis P, Agarwal N, Bellizzi M, Di Palma A.
    Pediatr Int; 2015 Oct 14; 57(5):1003-6. PubMed ID: 26286462
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  • 11. Mutational analysis of RUNX2 gene in Chinese patients with cleidocranial dysplasia.
    Zhang C, Zheng S, Wang Y, Zhao Y, Zhu J, Ge L.
    Mutagenesis; 2010 Nov 14; 25(6):589-94. PubMed ID: 20702542
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  • 12. 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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  • 13. Analysis of novel RUNX2 mutations in Chinese patients with cleidocranial dysplasia.
    Zhang X, Liu Y, Wang X, Sun X, Zhang C, Zheng S.
    PLoS One; 2017 Dec 31; 12(7):e0181653. PubMed ID: 28738062
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  • 14. [Mutation analysis of the RUNX2 gene in a family with cleidocranial dysplasia].
    Jiang T, Jiang X, Zhang Y.
    Hua Xi Kou Qiang Yi Xue Za Zhi; 2013 Oct 31; 31(5):522-5. PubMed ID: 24298808
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  • 15. 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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  • 16. A Novel 90-kbp Deletion of RUNX2 Associated with Cleidocranial Dysplasia.
    Zhang Y, Duan X.
    Genes (Basel); 2022 Jun 23; 13(7):. PubMed ID: 35885911
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  • 18. Identification of a Novel Splice Site Mutation in RUNX2 Gene in a Family with Rare Autosomal Dominant Cleidocranial Dysplasia.
    Jamali E, Khalesi R, Bitarafan F, Almadani N, Garshasbi M.
    Iran Biomed J; 2021 Jul 01; 25(4):297-302. PubMed ID: 34217160
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  • 19. Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.
    Jaruga A, Hordyjewska E, Kandzierski G, Tylzanowski P.
    Clin Genet; 2016 Nov 01; 90(5):393-402. PubMed ID: 27272193
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  • 20. Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia.
    Zhang T, Wu J, Zhao X, Hou F, Ma T, Wang H, Zhang X, Zhang X.
    Arch Oral Biol; 2019 Apr 01; 100():49-56. PubMed ID: 30798031
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