Search Results - Ehrbrecht, Antje

  • Showing 1 - 4 results of 4
Refine Results
  1. 1
    Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease

    Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease by Kubisch, Christian, Schoser, Benedikt G. H., Düring, Monika v., Betz, Regina C., Goebel, Hans-Hilmar, Zahn, Susanne, Ehrbrecht, Antje, Aasly, Jan, Schroers, Anja, Popovic, Nikola, Lochmüller, Hanns, Schröder, J. Michael, Brüning, Thomas, Malin, Jean-Pierre, Fricke, Britta, Meinck, Hans-Michael, Torbergsen, Torberg, Engels, Hartmut, Voss, Bruno, Vorgerd, Matthias

    Published in Annals of neurology
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1)

    Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1) by Zahn, Susanne, Ehrbrecht, Antje, Bosse, Kristin, Kalscheuer, Vera, Propping, Peter, Schwanitz, Gesa, Albrecht, Beate, Engels, Hartmut

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  3. 3
    P5: Genome-wide array-CGH screening of 52 patients with idiopathic mental retardation – Detection of two cases with de novo imbalances and two cases with causative imbalances inherited from a parent

    P5: Genome-wide array-CGH screening of 52 patients with idiopathic mental retardation – Detection of two cases with de novo imbalances and two cases with causative imbalances inher... by Ehrbrecht, Antje, Hoischen, Alexander, Ehrler, Marion, Bosse, Kristin, Pagenstecher, Constanze, Radlwimmer, Bernhard, Toedt, Grischa, Segraves, Richard, Pinkel, Daniel, Lichter, Peter, Weber, Ruthild G., Engels, Hartmut

    Get full text
    Article
    Save to List
    Saved in:
  4. 4
    P45: Comprehensive genomic analysis of desmoplastic medulloblastomas reveals novel amplified genes and supports a monoclonal origin of the different histologic components

    P45: Comprehensive genomic analysis of desmoplastic medulloblastomas reveals novel amplified genes and supports a monoclonal origin of the different histologic components by Hoischen, Alexander, Ehrbrecht, Antje, Mueller, Uta, Wolter, Marietta, Koch, Arend, Radlwimmer, Bernhard, Actor, Bertrand, Mincheva, Antoaneta, Pietsch, Torsten, Lichter, Peter, Reifenberger, Guido, Weber, Ruthild G.

    Get full text
    Article
    Save to List
    Saved in:

Search Tools: