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Journal Abstract Search

227 related items for PubMed ID: 28505335

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  • 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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  • 3. A novel 18-bp in-frame deletion mutation in RUNX2 causes cleidocranial dysplasia.
    Zeng L, Wei J, Zhao N, Sun S, Wang Y, Feng H.
    Arch Oral Biol; 2018 Dec; 96():243-248. PubMed ID: 29089101
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  • 6. Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case.
    Qin XY, Jia PZ, Zhao HX, Li WR, Chen F, Lin JX.
    Chin Med J (Engl); 2017 Jan 20; 130(2):165-170. PubMed ID: 28091408
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  • 7. A novel single-base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia.
    Pan Y, Lu W, Meng W, Liao W, Hu A, Wu B, Xiong F.
    Eur J Oral Sci; 2023 Feb 20; 131(1):e12910. PubMed ID: 36598486
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  • 8. 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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  • 10. Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype-phenotype correlations.
    Yoshida T, Kanegane H, Osato M, Yanagida M, Miyawaki T, Ito Y, Shigesada K.
    Blood Cells Mol Dis; 2003 Feb 07; 30(2):184-93. PubMed ID: 12732182
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  • 11. A novel small deletion mutation in RUNX2 gene in one Chinese family with cleidocranial dysplasia.
    Chen T, Hou J, Hu LL, Gao J, Wu BL.
    Int J Clin Exp Pathol; 2014 Feb 07; 7(5):2490-5. PubMed ID: 24966961
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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 Feb 07; 12(7):e0181653. PubMed ID: 28738062
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  • 14. 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 07; 37(5):772-776. PubMed ID: 29058294
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  • 15. Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations.
    Yoshida T, Kanegane H, Osato M, Yanagida M, Miyawaki T, Ito Y, Shigesada K.
    Am J Hum Genet; 2002 Oct 07; 71(4):724-38. PubMed ID: 12196916
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  • 19. RUNX2 mutation impairs osteogenic differentiation of dental follicle cells.
    Liu Y, Sun X, Zhang X, Wang X, Zhang C, Zheng S.
    Arch Oral Biol; 2019 Jan 07; 97():156-164. PubMed ID: 30391791
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