Hans Rudolf Lytchoff Eiberg

Hans Rudolf Lytchoff Eiberg

Associate Professor

ORCID: 0000-0002-4140-1578

Publication year:
All
1 - 5 out of 5Page size: 100
  1. 1994
  2. Published

    Assignment of Granular Corneal Dystrophy Groenouw Type 1 (CDGG1) to Chromosome 5q

    Eiberg, Hans Rudolf Lytchoff, Møller, H. U., Brendt, I. & Mohr, J., 1994, In: European Journal of Human Genetics. 2, p. 132-138

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

  3. Published

    Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis

    Eiberg, Hans Rudolf Lytchoff, Kjer, B., Kjer, P. & Rosenberg, T., 1994, In: Human Molecular Genetics. Vol 3, No 6, p. 977-980

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

  4. Published

    Gene for autosomale dominant congenital stationary night blindness maps to the same region as the gene for the *Gb-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3

    Gal, A., Xu, S., Duvigneau, C., Schwinger, E., Piczenik, Y., Rosenberg, T. & Eiberg, Hans Rudolf Lytchoff, 1994, In: Human Molecular Genetics. Vol 3, No 2, p. 323-325

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

  5. Published

    Linkage analysis between manic depressive illness and the dopamine beta-hydroxylase gene

    Ewald, H., Mors, O., Flint, T., Eiberg, Hans Rudolf Lytchoff & Kruse, T. A., 1994, In: Psychiatric Genetics. 4, p. 177-183

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

  6. Published

    Linkage analysis between manic-depressive illness and 35 classical markers

    Ewald, H., Mors, O. & Eiberg, Hans Rudolf Lytchoff, 1994, In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics. 54, p. 144-148

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

ID: 5291