Search Results - Brederlow, Benigna von

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  1. 1
    Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1D

    Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1D by von Brederlow, Benigna, Bolz, Hanno, Janecke, Andreas, La O Cabrera, Alicia, Rudolph, Günther, Lorenz, Birgit, Schwinger, Eberhard, Gal, Andreas

    Published in Human mutation
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  2. 2
    Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p

    Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p by Brederlow, Benigna von, Hahn, Angelika F., Koopman, Wilma J., Ebers, George C., Bulman, Dennis E.

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  3. 3
    Identification and in vitro expression of novelCDH23 mutations of patients with Usher syndrome type 1D

    Identification and in vitro expression of novelCDH23 mutations of patients with Usher syndrome type 1D by von Brederlow, Benigna, Bolz, Hanno, Janecke, Andreas, La O Cabrera, Alicia, Rudolph, G nther, Lorenz, Birgit, Schwinger, Eberhard, Gal, Andreas

    Published in Human mutation
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    Characterization of ADAMTS14, a novel member of the ADAMTS metalloproteinase family

    Characterization of ADAMTS14, a novel member of the ADAMTS metalloproteinase family by Bolz, Hanno, Ramı́rez, Alfredo, von Brederlow, Benigna, Kubisch, Christian

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