Hans Rudolf Lytchoff Eiberg
Associate Professor
Medical Genetics Program
Blegdamsvej 3, 2200 København N.
ORCID: 0000-0002-4140-1578
1 - 5 out of 5Page size: 10
- 2003
- Published
A novel mutation in the <epsilon>sarcoglycan gene causing myoclonus-Dystonia syndrome
Hjermind, L. E., Werdelin, L. M., Eiberg, Hans Rudolf Lytchoff, Kragh, O. B., Dupont, E. & Sørensen, S. A., 2003, In: Neurology. Vol. 60, p. 1536-1539Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Frequency of the HFE C282Y and H63D mutations in Danish patients with clinical haemochromatosis initially diagnosed by phenotypic methods
Milman, N., Koefoed, P., Pedersen, P., Nielsen, Finn Cilius & Eiberg, Hans Rudolf Lytchoff, 2003, In: European Journal of Haematology. 71, 6, p. 403-7 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genomic structure of the human mitochondrial chaperonin genes: HSP60 and HSP10 are localised head to head on chromosome 2 seperated by a bidirectional promoter
Hansen, J. J., Broos, P., Westergaard, M., Nielsen, M. N., Eiberg, Hans Rudolf Lytchoff, Børglum, A. D., Mogensen, J., Kristiansen, K., Bolund, L. & Gregersen, N., 2003, In: Hum. Genet.. Vol. 112, p. 71-77Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Heterogeneity of FeNO response to inhaled steroid in asthmatic children
Buchvald, F., Eiberg, Hans Rudolf Lytchoff & Bisgaard, H., 2003, In: Clin. Exp. Allergy. Vol. 33, p. 1735-1740Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Mutational analysis of the human FATE gene in 144 infertile men
Olesen, C., Silber, J., Eiberg, Hans Rudolf Lytchoff, Ernst, E., Petersen, K., Lindenberg, S. & Tommerup, Niels, 2003, In: Hum. Genet.. Vol. 113, p. 195-201Research 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
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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.
Research output: Contribution to journal › Journal article › Research › peer-review
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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