Hans Rudolf Lytchoff Eiberg
Associate Professor
Medical Genetics Program
Blegdamsvej 3, 2200 København N.
- 2004
- Published
Loss of heterozygosity at 9q33 and hypermethylation of the DBCCR1 gene in oral squamous cell carcinoma
Gao, S., Worm, J., Guldberg, P., Eiberg, Hans Rudolf Lytchoff, Krogdahl, A., Sorensen, Jette Led , Liu, C., Reibel, Jesper & Dabelsteen, Erik, 16 Aug 2004, In: B J C. 91, 4, p. 760-4 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetic and epigenetic alterations of the blood group ABO gene in oral squamous cell carcinoma
Gao, S., Worm, J., Guldberg, P., Eiberg, Hans Rudolf Lytchoff, Krogdahl, A., Liu, C., Reibel, Jesper & Dabelsteen, Erik, 20 Mar 2004, In: International journal of cancer. Journal international du cancer. 109, 2, p. 230-7 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cholestasis Familiaris Groenlandica / Byler-like disease in Greenland - A population study
Eiberg, Hans Rudolf Lytchoff, Nørgaard-Pedersen, B. & Nielsen, I., 2004, In: International Journal of Circumpolar Health. Vol. 63, suppl. 2, p. 189-191Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cholestasis Familiaris Groenlandica: an epidemiological, clinical and genetic study
Nielsen, I. M. & Eiberg, Hans Rudolf Lytchoff, 2004, In: International Journal of Circumpolar Health. Vol. 63, suppl. 2, p. 192-194Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetic and epigenetic alterations of the blood group ABO gene in oral squamous cell carcinoma
Gao, S., Worm, J., Guldberg, P., Eiberg, Hans Rudolf Lytchoff, Krogdahl, A., Liu, C. J., Reibel, J. & Dabelsteen, Erik, 2004, In: International Journal of Cancer. 109, p. 230-237Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Hereditary spastic paraplegia with cerebellar ataxia: a complex phenotype associated with a new SPG4 gene mutation.
Nielsen, Jørgen Erik, Johnson, B., Koefoed, P., Scheuer, K. H., Grønbech-Jensen, M., Law, I., Krabbe, K., Nørremølle, Anne, Eiberg, Hans Rudolf Lytchoff, Søndergård, H., Dam, M., Rehfeld, J. F., Krarup, C., Paulson, Olaf B., Hasholt, Lis Frydenreich & Sørensen, S. A., 2004, In: European Journal of Neurology. 11, 12, p. 817-824 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Loss of heterozygosity at 9q33 and hypermethylation of the DBCCRI gene in oral squamous cell carcinoma
Gao, S., Worm, J., Guldberg, P., Eiberg, Hans Rudolf Lytchoff, Krogdahl, A., Sørensen, J. A., Liu, C. J., Reibel, J. & Dabelsteen, E., 2004, In: British Journal of Cancer. Vol. 1-5, p. 10.1038/sj.bjc.6601980 - webResearch output: Contribution to journal › Journal article › Research › peer-review
- Published
Mosaicism of the CAG repeat sequence in the Huntington disease gene in a pair of monozygotic twins
Nørremølle, Anne, Hasholt, Lis Frydenreich, Petersen, C. B., Eiberg, Hans Rudolf Lytchoff, Hasselbalch, S. G., Gideon, P., Nielsen, J. E. & Sørensen, S. A., 2004, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 130, p. 154-159Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Mutation analysis of the Sonic hedgehog promoter and putative enhancer elements in Parkinson's disease patients
Bak, M., Hansen, C., Henriksen, K. F., Hansen, L., Pakkenberg, H., Eiberg, Hans Rudolf Lytchoff & Tommerup, Niels, 2004, In: Brain Research. Vol. 126, p. 207-211Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Novel Connexin 43(GJA1) mutation causes oculo-dento-digital dysplasia with curly hair
Kjær, K. W., Hansen, L., Eiberg, Hans Rudolf Lytchoff, Leicht, P., Opitz, J. M. & Tommerup, Niels, 2004, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 127A, p. 152-157Research output: Contribution to journal › Journal article › Research › peer-review
ID: 5291
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Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
1878
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A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
403
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Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
Research output: Contribution to journal › Letter › Research › peer-review
Published