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Journal Abstract Search

362 related items for PubMed ID: 21215027

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  • 5. Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.
    Lee B, Thirunavukkarasu K, Zhou L, Pastore L, Baldini A, Hecht J, Geoffroy V, Ducy P, Karsenty G.
    Nat Genet; 1997 Jul; 16(3):307-10. PubMed ID: 9207800
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  • 6. Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia.
    Quack I, Vonderstrass B, Stock M, Aylsworth AS, Becker A, Brueton L, Lee PJ, Majewski F, Mulliken JB, Suri M, Zenker M, Mundlos S, Otto F.
    Am J Hum Genet; 1999 Nov; 65(5):1268-78. PubMed ID: 10521292
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  • 10. [A Chinese girl with cleidocranial dysplasia (CCD) caused by the recurrent R190W mutation in RUNX 2].
    Qiu ZQ, Tang AL, Yu W, Ao Y, Wilson HY, Wei M, Zhang X.
    Zhonghua Er Ke Za Zhi; 2004 Oct; 42(10):759-61. PubMed ID: 16221346
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  • 11. 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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  • 12. Cleidocranial dysplasia: clinical and molecular genetics.
    Mundlos S.
    J Med Genet; 1999 Mar; 36(3):177-82. PubMed ID: 10204840
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  • 13. 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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  • 14. A Case of Cleidocranial Dysplasia with a Novel Mutation and Growth Velocity Gain with Growth Hormone Treatment.
    Çamtosun E, Akıncı A, Demiral E, Tekedereli İ, Sığırcı A.
    J Clin Res Pediatr Endocrinol; 2019 Sep 03; 11(3):301-305. PubMed ID: 30468148
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  • 17. 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 03; 49(6):435-42. PubMed ID: 15099800
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  • 18. Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.
    Jaruga A, Hordyjewska E, Kandzierski G, Tylzanowski P.
    Clin Genet; 2016 Nov 03; 90(5):393-402. PubMed ID: 27272193
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  • 20. Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2 : possible involvement of non-genetic or epigenetic regulation.
    Suda N, Hamada T, Hattori M, Torii C, Kosaki K, Moriyama K.
    Orthod Craniofac Res; 2007 Nov 03; 10(4):222-5. PubMed ID: 17973689
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