檢索結果 - Beate Mitulla

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    “Mowat‐Wilson” syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies‐mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene

    “Mowat‐Wilson” syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies‐mental retardation syndrome caused by mutations in the zinc... 由 Christiane Zweier, Beate Albrecht, Beate Mitulla, R. Behrens, Maike Beese, Gabriele Gillessen‐Kaesbach, Hans‐Dieter Rott, Anita Rauch

    出版 2002
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    Molecular Analysis of SALL1 Mutations in Townes-Brocks Syndrome

    Molecular Analysis of SALL1 Mutations in Townes-Brocks Syndrome 由 Jürgen Kohlhase, Peter E.M. Taschner, Peter Burfeind, Bastian Pasche, William G. Newman, Christopher Blanck, Martijn H. Breuning, Leo P. ten Kate, P. D. Maaswinkel-Mooy, Beate Mitulla, Jörg Seidel, Susan J. Kirkpatrick, Richard M. Pauli, David S. Wargowski, Koenraad Devriendt, Willem Proesmans, Orazio Gabrielli, Giovanni V. Coppa, Eveline Wesby–van Swaay, Richard C. Trembath, Albert Schinzel, William Reardon, E Seemanová, Wolfgang Engel

    出版 1999
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