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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

120 related items for PubMed ID: 12650905

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  • 25. X-linked spondyloepiphyseal dysplasia tarda: molecular cause of a heritable disorder associated with early degenerative joint disease.
    Fiedler J, Bergmann C, Brenner RE.
    Acta Orthop Scand; 2003 Dec; 74(6):737-41. PubMed ID: 14763708
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  • 27. Spondyloepiphyseal dysplasia tarda: report of one case.
    Shu SG, Tsai CR, Chi CS.
    Acta Paediatr Taiwan; 2002 Dec; 43(2):106-8. PubMed ID: 12041616
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  • 30. Gene structure and expression study of the SEDL gene for spondyloepiphyseal dysplasia tarda.
    Gécz J, Hillman MA, Gedeon AK, Cox TC, Baker E, Mulley JC.
    Genomics; 2000 Oct 15; 69(2):242-51. PubMed ID: 11031107
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  • 36. [Pathology and molecular pathogenesis of spondyloepiphyseal dysplasia tarda with progressive arthropathy caused by compound CCN6 heterogeneous gene mutations].
    Peng YQ, Liao EY, Gu HM, Wei QY, Zhou HD, Li J, Xie H, Zhai MX, Tan LH, Luo XH, Wu XP, Hu PA, Ni JD, Su X, Jiang Y, Dai RC, Guo LJ, Yuan LQ, Wang M, Wang PF, Liu SP, Yang Y, Wang C, Sui GL, Fang TY.
    Zhonghua Yi Xue Za Zhi; 2004 Nov 02; 84(21):1796-803. PubMed ID: 15631777
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  • 37. Novel TRAPPC2 mutation in a boy with X-linked spondylo-epiphyseal dysplasia tarda.
    Adachi H, Takahashi I, Takahashi T.
    Pediatr Int; 2014 Dec 02; 56(6):925-928. PubMed ID: 25521980
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