Hans Rudolf Lytchoff Eiberg

Hans Rudolf Lytchoff Eiberg

Associate Professor

ORCID: 0000-0002-4140-1578

Publication year:
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1 - 6 out of 6Page size: 10
  1. 2005
  2. 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

  3. Published

    Cytoplasmic expression of E-cadherin and β-Catenin correlated with LOH and hypermethylation of the APC gene in oral squamous cell carcinomas

    Gao, S., Eiberg, Hans Rudolf Lytchoff, Krogdahl, A., Lui, C. & Sørensen, J. A., 2005, In: J. Oral. Pathol. Med.. Vol. 34, p. 116-119

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

  4. Published

    Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)

    Kjær, K. W., Hansen, L., Schwabe, G. C., Marques-de-Faria, A. P., Eiberg, Hans Rudolf Lytchoff, Mundlos, S., Tommerup, Niels & Rosenberg, T., 2005, In: Journal of Medical Genetics. Vol. 42, p. 292-298

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

  5. 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

  6. 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

  7. 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

ID: 5291