Lars Allan Larsen

Lars Allan Larsen

Professor

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    Publication year:
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    1 - 7 out of 7Page size: 10
    1. 2004
    2. Published

      Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome

      Boonen, S. E., Stahl, D., Kreiborg, Sven, Rosenberg, T., Kalscheuer, V., Larsen, Lars Allan, Tommerup, Niels, Brøndum-Nielsen, K. & Tümer, Asuman Zeynep, 2004, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 132A, p. 324-328

      Research output: Contribution to journal › Journal article › Research › peer-review

    3. Published

      Does KCNE5 play a role in long QT syndrome?

      Hofman-Bang, J., Jespersen, Thomas, Grunnet, Morten, Larsen, Lars Allan, Andersen, P. S., Kanters, Jørgen K., Kjeldsen, K. & Christiansen, M., 2004, In: Clinica Chimica Acta. 345, 1-2, p. 49-53 4 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    4. Published

      GJB2 and GJB6 mutations in 165 Danish patients showing non-syndromic hearing impairment

      Grønskov, K., Larsen, Lars Allan, Rendtorff, N. D., Parving, A., Nørgaard-Pedersen, B. & Brøndum-Nielsen, K., 2004, In: Genet Test. Vol. 8, p. 181-184

      Research output: Contribution to journal › Journal article › Research › peer-review

    5. Published

      Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency

      Andersen, P. S., Havndrup, O., Bundgaard, H., Larsen, Lars Allan, Vuust, J., Pedersen, A. K., Kjeldsen, K. & Christiansen, M., 2004, In: European Journal of Human Genetics. Vol. 12, p. 673-677

      Research output: Contribution to journal › Journal article › Research › peer-review

    6. Published

      High Throughput Mutation Screening

      Andersen, P. S. & Larsen, Lars Allan, 2004, Molecular Analysis and Genome Discovery. New York: IEEE Computer Society Press, p. chap. 5

      Research output: Chapter in Book/Report/Conference proceeding › Report chapter › Research

    7. Published

      Identification of a novel EYA1 splice-site mutation in a Danish branchio-oto-renal syndrome family

      Henriksen, A. M., Tümer, Asuman Zeynep, Tommerup, Niels, Tranebjærg, Lisbeth & Larsen, Lars Allan, 2004, In: Genetic Testing. 8, 4, p. 404-6 2 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    8. Published

      T wave morphology analysis distinguishes between KvLQT1 and HERG mutations in long QT syndrome

      Kanters, J. K., Fanoe, S., Larsen, Lars Allan, Bloch-Thomsen, P. E., Toft, E. & Christansen, M., 2004, In: Heart Rhythm. Vol. 1, p. 285-292

      Research output: Contribution to journal › Journal article › Research › peer-review

    ID: 2949