Search Results - Rödl, Tanja

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  1. 1
    Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders

    Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders by Geis, Tobias, Rödl, Tanja, Topaloğlu, Haluk, Balci-Hayta, Burcu, Hinreiner, Sophie, Müller-Felber, Wolfgang, Schoser, Benedikt, Mehraein, Yasmin, Hübner, Angela, Zirn, Birgit, Hoopmann, Markus, Reutter, Heiko, Mowat, David, Schuierer, Gerhard, Schara, Ulrike, Hehr, Ute, Kölbel, Heike

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  2. 2
    Homozygous dystroglycan mutation associated with a novel muscle–eye–brain disease-like phenotype with multicystic leucodystrophy

    Homozygous dystroglycan mutation associated with a novel muscle–eye–brain disease-like phenotype with multicystic leucodystrophy by Geis, Tobias, Marquard, Klaus, Rödl, Tanja, Reihle, Christof, Schirmer, Sophie, von Kalle, Thekla, Bornemann, Antje, Hehr, Ute, Blankenburg, Markus

    Published in Neurogenetics
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  3. 3
    Das soziale Defizit des Europäischen Integrationsprojekts

    Das soziale Defizit des Europäischen Integrationsprojekts by Joerges, Christian, Rödl, Florian

    Published in Kritische Justiz
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