Lars Hansen

Lars Hansen

Visiting researcher

Member of:


    1. 2012
    2. Published

      Novel mutation in ATP13A2 widens the spectrum of Kufor-Rakeb syndrome (PARK9)

      Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Korbo, L., Nielsen, I., Svenstrup, K., Bech, S., Pinborg, L., Friberg, L., Hjermind, L., Olsen, O. & Nielsen, Jørgen Erik, Nov 2012, In: Clinical Genetics. 82, 3, p. 256-63 8 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    3. Published

      Author response: Nonspecific PCR amplification of CRYBB2-pseudogene leads to misconception of natural variation as mutation

      Hansen, Lars & Rosenberg, T., 1 Sep 2012, In: Investigative Ophthalmology and Visual Science. 53, 10, 1 p., 6666.

      Research output: Contribution to journalComment/debateResearchpeer-review

    4. Published

      Genetic studies in congenital anterior midline cervical cleft

      Jakobsen, Linda Plovmand, Pfeiffer, P., Andersen, M., Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Mang, Y., Bak, M., Møller, R. S., Klitten, L. L. & Tommerup, Niels, Aug 2012, In: American Journal of Medical Genetics. Part A. 158A, 8, p. 2021-6 6 p.

      Research output: Contribution to journalJournal articleResearchpeer-review

    ID: 544414