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Journal Abstract Search

123 related items for PubMed ID: 16329826

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  • 10. [Identification of three novel frameshift mutations in the RUNX2 gene in three sporadic Chinese cases with cleidocranial dysplasia].
    Qi Z, Yang W, Meng Y, Liu Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug; 31(4):415-9. PubMed ID: 25119901
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  • 12. 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; 25(6):589-94. PubMed ID: 20702542
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  • 16. PEBP2alphaA/CBFA1 mutations in Japanese cleidocranial dysplasia patients.
    Zhang YW, Yasui N, Kakazu N, Abe T, Takada K, Imai S, Sato M, Nomura S, Ochi T, Okuzumi S, Nogami H, Nagai T, Ohashi H, Ito Y.
    Gene; 2000 Feb 22; 244(1-2):21-8. PubMed ID: 10689183
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  • 17. Identification of a stop codon mutation in the CBFA1 runt domain from a patient with cleidocranial dysplasia and cleft lip.
    Yamachika E, Tsujigiwa H, Ishiwari Y, Mizukawa N, Nagai N, Sugahara T.
    J Oral Pathol Med; 2001 Jul 22; 30(6):381-3. PubMed ID: 11459326
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  • 20. Novel mutation of RUNX2 gene in a patient with cleidocranial dysplasia.
    Guo YW, Chiu CY, Liu CL, Jap TS, Lin LY.
    Int J Clin Exp Pathol; 2015 Jul 22; 8(1):1057-62. PubMed ID: 25755819
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