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Journal Abstract Search

161 related items for PubMed ID: 14763708

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  • 3. Preonset studies of spondyloepiphyseal dysplasia tarda caused by a novel 2-base pair deletion in SEDL encoding sedlin.
    Mumm S, Zhang X, Gottesman GS, McAlister WH, Whyte MP.
    J Bone Miner Res; 2001 Dec; 16(12):2245-50. PubMed ID: 11760838
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  • 7. Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda.
    Christie PT, Curley A, Nesbit MA, Chapman C, Genet S, Harper PS, Keeling SL, Wilkie AO, Winter RM, Thakker RV.
    J Clin Endocrinol Metab; 2001 Jul; 86(7):3233-6. PubMed ID: 11443194
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  • 8. [Gene diagnosis of X-linked spondyloepiphyseal dysplasia tarda by linkage analysis and DNA sequencing].
    Wang HL, Gao C, Luo Q, Sheng GY, Zhou JH, Gao TZ, Peng S, Lu JP.
    Zhonghua Er Ke Za Zhi; 2003 Apr; 41(4):256-9. PubMed ID: 14754526
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  • 12. [Mutational analysis in a family with X-linked spondyloepiphyseal dysplasia tarda].
    Zhu HY, Li J, Zhu RF, Wu X, Duan HL, Yang Y, Zhang Y, Hu Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Aug; 25(4):421-3. PubMed ID: 18683141
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  • 13. X-linked recessive spondyloepiphyseal dysplasia tarda. Clinical and radiographic evolution in a 6-generation kindred and review of the literature.
    Whyte MP, Gottesman GS, Eddy MC, McAlister WH.
    Medicine (Baltimore); 1999 Jan; 78(1):9-25. PubMed ID: 9990351
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  • 16. X-linked spondyloepiphyseal dysplasia tarda: a novel SEDL mutation in a Jewish Ashkenazi family and clinical intervention considerations.
    Bar-Yosef U, Ohana E, Hershkovitz E, Perlmuter S, Ofir R, Birk OS.
    Am J Med Genet A; 2004 Feb 15; 125A(1):45-8. PubMed ID: 14755465
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  • 18. Spondyloepiphyseal dysplasia tarda. The autosomal recessive form in two sisters.
    Ikegawa S.
    Arch Orthop Trauma Surg; 1993 Feb 15; 113(1):49-52. PubMed ID: 8117511
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