Showing 1 - 3 results of 3 for search 'Brøndum-Nielsen Karen', query time: 0.01s Refine Results
  1. 1
    Genomic deletions in <it>OPA1 </it>in Danish patients with autosomal dominant optic atrophy

    Genomic deletions in <it>OPA1 </it>in Danish patients with autosomal dominant optic atrophy by Larsen Michael, Milea Dan, Grønskov Karen, Almind Gitte J, Brøndum-Nielsen Karen, Ek Jakob

    Published 2011
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  2. 2
    Dominant optic atrophy in Denmark - report of 15 novel mutations in <it>OPA1</it>, using a strategy with a detection rate of 90%

    Dominant optic atrophy in Denmark - report of 15 novel mutations in <it>OPA1</it>, using a strategy with a detection rate of 90% by Almind Gitte J, Ek Jakob, Rosenberg Thomas, Eiberg Hans, Larsen Michael, LuCamp LuCamp, Brøndum-Nielsen Karen, Grønskov Karen

    Published 2012
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  3. 3
    Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter

    Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5q... by Tommerup Niels, Baekgaard Peter, Pedersen Vibeke, Ledaal Paal, Friis Birgitte, Hahnemann Johanne, Hjalgrim Helle, Tümer Zeynep, Sogaard Marie, Cingöz Sultan, Duno Morten, Brondum-Nielsen Karen

    Published 2005
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