نتائج البحث - Beate Mitulla

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  1. 1
    “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... حسب Christiane Zweier, Beate Albrecht, Beate Mitulla, R. Behrens, Maike Beese, Gabriele Gillessen‐Kaesbach, Hans‐Dieter Rott, Anita Rauch

    منشور في 2002
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  2. 2
    Molecular Analysis of SALL1 Mutations in Townes-Brocks Syndrome

    Molecular Analysis of SALL1 Mutations in Townes-Brocks Syndrome حسب 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

    منشور في 1999
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