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. 2010
  2. Published

    Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS

    Farooq, M., Troelsen, J. T., Boyd, M., Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hussain, M. S., Rehman, S. U., Azhar, A., Ali, A., Bakhtiar, S. M., Tommerup, Niels, Baig, S. M. & Kjaer, K. W., Jun 2010, In: European Journal of Human Genetics. 18, 6, p. 733-6 3 p.

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

  3. Published

    A mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani family

    Anjum, I., Eiberg, Hans Rudolf Lytchoff, Baig, S. M., Tommerup, Niels & Hansen, Lars, Mar 2010, In: Molecular Vision. 16, p. 549-55 6 p.

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

  4. Published

    Human eye colour and HERC2, OCA2 and MATP

    Mengel-From, J., Børsting, Claus, Sanchez, J. J., Eiberg, Hans Rudolf Lytchoff & Morling, Niels, 12 Jan 2010, In: Forensic Science International: Genetics. 4, 5, p. 323 - 328 6 p.

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

  5. Published

    Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity

    Gjesing, A. P., Larsen, L. H., Torekov, S. S., Hainerová, I. A., Kapur, R., Johansen, A., Albrechtsen, A., Boj, S., Holst, B., Harper, A., Urhammer, S. A., Borch-Johnsen, K., Pisinger, C. H., Echwald, S. M., Eiberg, H. R. L., Astrup, A., Lebl, J., Ferrer, J., Schwartz, T. W., Hansen, T. & 1 others, Pedersen, Oluf Borbye, 2010, In: P L o S One. 5, 4, 8 p.

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

  6. Published

    Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation

    Bech, S., Petersen, T., Nørremølle, Anne, Gjedde, Albert, Ehlers, L., Eiberg, Hans Rudolf Lytchoff, Hjermind, L. E., Hasholt, Lis Frydenreich, Lundorf, E. & Nielsen, Jørgen Erik, 2010, In: Parkinsonism & Related Disorders. 16, 1, p. 12-5 3 p.

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

  7. Published

    Prænatal screening for leversygdommen (CFG) og stofskiftesygdommen (PCCB)

    Nielsen, I., Bisgaard, S. M. L. & Eiberg, Hans Rudolf Lytchoff, 2010, In: Nakorsanut. 1, p. 12-17 6 p.

    Research output: Contribution to journal › Journal article › Research

ID: 5291