Hans Rudolf Lytchoff Eiberg

Hans Rudolf Lytchoff Eiberg

Associate Professor

ORCID: 0000-0002-4140-1578

Publication year:
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171 - 180 out of 189Page size: 10
  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

  7. 1993
  8. Published

    A silent A to G mutation in exon 11 of the medium-chain acyl-CoA dehydrogenase (MCAD) gene

    Andresen, B. S., Kølvraa, S., Bross, P., Bolund, L., Curtis, D., Eiberg, Hans Rudolf Lytchoff, Zhang, Z., Kelly, D. P., Strauss, A. W. & Gregersen, N., 1993, In: Human Molecular Genetics. 2, p. 4

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

  9. Published

    Linkage Studies of Cholestasis Familiaris Groenlandica/Byler-like Disease with Polymorphic Protein and Blood Markers

    Eiberg, Hans Rudolf Lytchoff & Nielsen, I., 1993, In: Human Heredity. 43, p. 250-256

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

  10. Published

    Suggestion of linkage between manic-depressive illness and the enzyme phosphoglycolate phosphatase (PGP) on chromosome 16p

    Eiberg, Hans Rudolf Lytchoff, Ewald, H. & Mors, O., 1993, In: Clinical Genetics. 44, p. 254-257

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

  11. 1992
  12. Published

    Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneity

    Lund, A. M., Eiberg, Hans Rudolf Lytchoff, Rosenberg, T. & Warburg, M., 1992, In: Clinical Genetics. 41, p. 65-69

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

  13. Published

    Præklinisk og prænatal diagnostik af familiær adenomatøs polypose

    Bisgaard, M. L., Bülow, S., Winther, K., Eiberg, Hans Rudolf Lytchoff, Niebuhr, E. & Mohr, J., 1992, In: Ugeskrift for læger. 154, p. 921-924

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

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