Clinical and mutational spectrum of Mowat-Wilson syndrome

C. Zweier, C.T. Thiel, A. Dufke, Y.J. Crow, P. Meinecke, M. Suri, S. Ala-Mello, F. Beemer, S. Bernasconi, P. Bianchi, A. Bier, K. Devriendt, B. Dimitrov, H. Firth, R.C. Gallagher, L. Garavelli, G. Gillessen-Kaesbach, L. Hudgins, H. Kaariainen, S. KarstensI. Krantz, A. Mannhardt, L. Medne, J. Mucke, M. Kibaek, L.N. Krogh, M. Peippo, O. Rittinger, S. Schulz, S.L. Schelley, I.K. Temple, N.R. Dennis, M.S. van der Knaap, P. Wheeler, B. Yerushalmi, M. Zenker, H. Seidel, A. Lachmeijer, T. Prescott, C. Kraus, R.B. Lowry, A. Rauch

Research output: Contribution to JournalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)97-111
JournalEuropean Journal of Medical Genetics
Volume48
Issue number2
DOIs
Publication statusPublished - 2005
Externally publishedYes

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