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

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