Showing 1 - 2 results of 2 for search 'Stemmler Susanne', query time: 0.01s Refine Results
  1. 1
    Autosomal dominant hereditary spastic paraplegia: Novel mutations in the <it>REEP1 </it>gene (SPG31)

    Autosomal dominant hereditary spastic paraplegia: Novel mutations in the <it>REEP1 </it>gene (SPG31) by Epplen Joerg T, Arning Larissa, Schlang Katharina J, Stemmler Susanne

    Published 2008
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  2. 2
    Evaluation of the toll-like receptor 6 Ser249Pro polymorphism in patients with asthma, atopic dermatitis and chronic obstructive pulmonary disease

    Evaluation of the toll-like receptor 6 Ser249Pro polymorphism in patients with asthma, atopic dermatitis and chronic obstructive pulmonary disease by Reinitz-Rademacher Karin, Rohde Gernot, Arinir Umut, Petrasch-Parwez Elisabeth, Parwez Qumar, Stemmler Susanne, Hoffjan Sabine, Schultze-Werninghaus Gerhard, Bufe Albrecht, Epplen Jörg T

    Published 2005
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