Hans Rudolf Lytchoff Eiberg
Associate Professor
Medical Genetics Program
Blegdamsvej 3, 2200 København N.
- 1997
- Published
(1997) Clinical enuresis phenotypes in familial nocturnal enuresis
Gontard, A. V., Hollmann, E., Benden, B., Eiberg, Hans Rudolf Lytchoff, Rittig, S. & Lehmkuhl, G., 1997, In: Scandinavian Journal of Urology and Nephrology. 31 (suppl.183), p. 11-16Research output: Contribution to journal › Journal article › Research › peer-review
- Published
A Survey of the Newborn Populations in Belgium, Germany, Poland, Czech Republic, Hungary, Bulgaria, Spain, Turkey and Japan for the G985 Variant Allele with Haplotype Analysis at the Medium Chain Acyl-CoA Dehydrogenase Gene. Locus: Clinical and Evol.Con.
Tanaka, K., Gregersen, N., Ribes, A., Kim, J., Kølvraa, S., Winter, V. S., Eiberg, Hans Rudolf Lytchoff, Martinez, G., Deufel, T., Leifert, B., Santer, R., Francois, B., Pronicka, E., Laszlo, A., Kmoch, S., Kremensky, I., Kalaydjicva, L., Ozalp, I. & Ito, M., 1997, In: Pediatric Research. vol 41, 2, p. 201-209Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Assignment of human plasma methylumbelliferyl-tetra-N-acetylchitotetraoside hydrolase or chitinase to chromosome 1 q by a linkage study
Eiberg, Hans Rudolf Lytchoff & Tandt, W. R. D., 1997, In: Human Genetics. 101, p. 205-207Research output: Contribution to journal › Journal article › Research › peer-review
- Published
CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24
Nielsen, J. E., Koefoed, P., Abell, K., Eiberg, Hans Rudolf Lytchoff, Fenger, K., Niebuhr, E. & Sørensen, S. A., 1997, In: Human Molecular Genetics. Vol. 6, No. 11, p. 1811-1816Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Clinical enuresis phenotypes in familial nocturnal enuresis
von Gontard, A., Hollmann, E., Benden, B., Eiberg, Hans Rudolf Lytchoff, Rittig, S. & Lehmkuhl, G., 1997, In: Scandinavian Journal of Urology and Nephrology. 31 (suppl. 183), p. 11-16Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Genetic Heterogeneity in Nocturnal Enuresis
Gontard, A. V., Eiberg, Hans Rudolf Lytchoff, Hollmann, E., Rittig, S. & Lehmkuhl, G., 1997, In: American Journal of Psychiatry. 153, p. 885Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Novel Mody3 Mutations in the Hepatocyte Factor-1a Gene. Evidence for a Hyperexcitabillity of Pancreatic ß-cells to Intravenous Secretagogues in a Glucosetolerant Carrier of a P447L Mutation
Hansen, T., Eiberg, Hans Rudolf Lytchoff, Rouard, M., Vaxillaire, M., Møller, A. M., Rasmussen, S. K., Fridberg, M. & Holst, Jens Juul, 1997, In: Diabetes. 46, p. 726-730Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Refinement of the dominant optic atrophy locus (OPA1) to a 1,4-cM interval on chromosome 3q28-3q29, within a 3-Mb YAC contig
Jonasdottir, A., Eiberg, Hans Rudolf Lytchoff, Kjer, B., Kjer, P. & Rosenberg, T., 1997, In: Human Genetics. 99, p. 115-120Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Structural organization of the human short-chain acyl-CoA dehydrogenase gene
Corydon, M. J., Andresen, B. S., Bross, P., Kjeldsen, M., Andreasen, P. H., Eiberg, Hans Rudolf Lytchoff, Kølvraa, S. & Gregersen, N., 1997, In: Mammalian Genome. 8, p. 922-926Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Susceptibility loci for bipolar affective disorder on chromosome 18? A review and a study of Danish families
Ewald, H., Mors, O., Koed, K., Eiberg, Hans Rudolf Lytchoff & Kruse, T. A., 1997, In: Psychiatric Genetics. 7, p. 1-12Research 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
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