Works matching IS 19466234 AND DT 2010 AND VI 2 AND IP 23

Results: 4
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    Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome.

    Published in:
    Science Translational Medicine, 2010, v. 2, n. 23, p. 1, doi. 10.1126/scitranslmed.3000488
    By:
    • Loeys, B. L.;
    • Gerber, E. E.;
    • Riegert-Johnson, D.;
    • Iqbal, S.;
    • Whiteman, P.;
    • McConnell, V.;
    • Chillakuri, C. R.;
    • Macaya, D.;
    • Coucke, P. J.;
    • De Paepe, A.;
    • Judge, D. P.;
    • Wigley, F.;
    • Davis, E. C.;
    • Mardon, H. J.;
    • Handford, P.;
    • Keene, D. R.;
    • Sakai, L. Y.;
    • Dietz, H. C.
    Publication type:
    Article
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