Lars Hansen

Lars Hansen

Guest Researcher


Publication year:
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51 - 59 out of 59Page size: 10
  1. 2006
  2. Published

    A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2

    Kjær, K. W., Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hagen, C. B. V. D., Rosendahl, K., Tommerup, Niels & Mundlos, S., 2006, In: Journal of Medical Genetics. 43, 3, p. 225-231 6 p.

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

  3. Published

    Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene

    Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Kjer, B., Hansen, T., Pedersen, O., Bille, M., Rosenberg, T. & Tranebjaerg, L., 2006, In: Journal of Medical Genetics. 43, 5, p. 435-440 5 p.

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

  4. Published

    The congenital "ant-egg" cataract phenotype is caused by a missense mutation in connexin46

    Hansen, Lars, Yao, W., Eiberg, Hans Rudolf Lytchoff, Funding, M., Riise, R., Kjær, K. W., Hejtmancik, J. F. & Rosenberg, T., 2006, In: Molecular Vision. 12, 116, p. 1033-1039 7 p.

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

  5. 2005
  6. Published

    Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1

    Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hansen, C., Mohr, J., Teglbjærg, P. S. & Kjaer, K. W., 15 Feb 2005, In: American Journal of Medical Genetics. 133 A, 1, p. 44-47 4 p.

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

  7. Published

    A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions

    Kjær, K. W., Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Utkus, A., Skovgaard, Lene Theil, Leicht, P., Opitz, J. M. & Tommerup, Niels, 2005, In: American Journal of Medical Genetics. Part A. 138, 4, p. 328-39 12 p.

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

  8. Published

    Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARG

    Kjaer, K. W., Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Christensen, K. S., Opitz, J. M. & Tommerup, Niels, 2005, In: American Journal of Medical Genetics. Part A. 137, 2, p. 148-52 4 p.

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

  9. Published

    Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified

    Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Barrett, T., Bek, T., Kjærsgaard, P., Tranebjærg, Lisbeth & Rosenberg, T., 2005, In: European Journal of Human Genetics. 13, 12, p. 1275-1284

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

  10. 1991
  11. Published

    The barley genes acl1 and Acl3 encoding acyl carrier proteins I and III are located on different chromosomes

    Hansen, Lars & von Wettstein-Knowles, P., Oct 1991, In: MGG Molecular & General Genetics. 229, 3, p. 467-478 12 p.

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

  12. 1987
  13. Published

    Three cDNA clones for barley leaf acyl carrier proteins I and III

    Hansen, Lars, Nov 1987, In: Carlsberg Research Communications. 52, 6, p. 381-392 12 p.

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

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ID: 544414