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Journal Abstract Search

195 related items for PubMed ID: 11127404

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  • 4. [A splicing mutation of EXT1 in a Chinese pedigree with hereditary multiple exostoses].
    Wang W, Qiu ZQ, Song HM.
    Zhongguo Dang Dai Er Ke Za Zhi; 2014 Feb; 16(2):174-80. PubMed ID: 24568913
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  • 6. Novel EXT1 and EXT2 mutations in hereditary multiple exostoses families of Indian origin.
    Vanita V, Sperling K, Sandhu HS, Sandhu PS, Singh JR.
    Genet Test Mol Biomarkers; 2009 Feb; 13(1):43-9. PubMed ID: 19309273
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  • 10. Coexistence of hereditary multiple exostoses and ankylosing spondylitis.
    Olmez N, Günaydin R, Gürgan A, Elçin F.
    Clin Rheumatol; 1999 Feb; 18(6):481-4. PubMed ID: 10638774
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  • 11. Hereditary multiple and isolated sporadic exostoses in the same kindred: identification of the causative gene (EXT2) and detection of a new mutation, nt112delAT, that distinguishes the two phenotypes.
    Vujic M, Bergman A, Romanus B, Wahlström J, Martinsson T.
    Int J Mol Med; 2004 Jan; 13(1):47-52. PubMed ID: 14654969
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  • 14. The type 2 diabetes associated rs7903146 T allele within TCF7L2 is significantly under-represented in Hereditary Multiple Exostoses: insights into pathogenesis.
    Sgariglia F, Pedrini E, Bradfield JP, Bhatti TR, D'Adamo P, Dormans JP, Gunawardena AT, Hakonarson H, Hecht JT, Sangiorgi L, Pacifici M, Enomoto-Iwamoto M, Grant SF.
    Bone; 2015 Mar; 72():123-7. PubMed ID: 25498973
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  • 16. Hereditary multiple exostoses causing cord compression.
    Bari MS, Jahangir Alam MM, Chowdhury FR, Dhar PB, Begum A.
    J Coll Physicians Surg Pak; 2012 Dec; 22(12):797-9. PubMed ID: 23217490
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  • 20. [Hereditary multiple exostoses. Molecular genetic analysis of the EXT1 gene in an unusual family].
    Heinritz W, Pretzsch M, Koall S, Matzen PF, Froster UG.
    Orthopade; 2005 May; 34(5):470-6. PubMed ID: 15739063
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