Showing 1 - 4 results of 4 for search 'Epplen Joerg T', query time: 0.02s 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
    Connect to this object online.
    Book
    Save to List
    Saved in:
  2. 2
    <it>PTPRC</it> (CD45) is not associated with multiple sclerosis in a large cohort of German patients

    <it>PTPRC</it> (CD45) is not associated with multiple sclerosis in a large cohort of German patients by Haupts Michael, Sindern Eckhart, Miterski Bianca, Schimrigk Sebastian, Epplen Joerg T

    Published 2002
    Connect to this object online.
    Book
    Save to List
    Saved in:
  3. 3
    On the Wegener granulomatosis associated region on chromosome 6p21.3

    On the Wegener granulomatosis associated region on chromosome 6p21.3 by Csernok Elena, Jagiello Peter, Szyld Paweł, Gross Wolfgang L, Epplen Joerg T

    Published 2006
    Connect to this object online.
    Book
    Save to List
    Saved in:
  4. 4
    HNPCC: Six new pathogenic mutations

    HNPCC: Six new pathogenic mutations by Epplen Joerg T, Hahn Stephan A, Brasch Frank E, Vieland Judith, Kunstmann Erdmute, Schulmann Karsten, Schmiegel Wolff

    Published 2004
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: