Hans Rudolf Lytchoff Eiberg
Associate Professor
Medical Genetics Program
Blegdamsvej 3, 2200 København N.
ORCID: 0000-0002-4140-1578
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- 2000
- Published
A missense mutation in F1C1 is associated with Greenland familial cholestasis
Klomp, L. W. J., Bull, L. N., Knisely, A. S., van der Doelen, M. A. M., Juijn, J. A., Berger, R., Forget, S., Nielsen, I., Eiberg, Hans Rudolf Lytchoff & Houwen, R. H. J., 2000, In: Hepatology. Vol.32, p. 1337-1341Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Epidermolysis bullosa simplex: Korrelation mellem genotype og fænotype hos danske patienter.
Sørensen, C. B., Ladekjær-Mikkelsen, A., Andresen, B. S., Brandrup, F., Veien, N. K., Buus, S. K., Anton-Lamprecht, I., Kruse, T. A., Jensen, P. K. A., Eiberg, Hans Rudolf Lytchoff, Bolund, L. & Gregersen, N., 2000, In: Ugeskrift for læger. 162/13, p. 1873-1876Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene
Eksandh, L., Ponjavic, V., Munroe, P. B., Eiberg, Hans Rudolf Lytchoff, Uvebrant, P., Ehinger, B., Mole, S. E. & Andréasson, S., 2000, In: Ophthalmic Genetics. 71,2 pp., p. 69-77Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Linkage of cholestasis familiaris Groenlandica/Byler-like disease to chromosome 18
Eiberg, Hans Rudolf Lytchoff & Nielsen, I., 2000, In: International Journal of Circumpolar Health. 59, p. 57-62Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Missense mutations in the human insulin promoter factor-1 gene and their relation to maturity-onset diabetes of the young and late-onset type 2 diabetes mellitus in caucasians
Hansen, L., Urioste, S., Petersen, H. V., Jensen, J. N., Eiberg, Hans Rudolf Lytchoff, Barbetti, F., Serup, P., Hansen, T. & Pedersen, O., 2000, In: Journal of Clinical Endocrinology and Metabolism. 85, 3, p. 1323-1326Research output: Contribution to journal › Journal article › Research › peer-review
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Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity
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1878
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A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
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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