Hans Rudolf Lytchoff Eiberg
Associate Professor
Medical Genetics Program
Blegdamsvej 3, 2200 København N.
- 1997
- 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
- 1996
- Published
A linkage study between maniodepressive illness and chromsome 21
Ewald, H., Eiberg, Hans Rudolf Lytchoff, Mors, O., Flint, T. & Kruse, T. A., 1996, In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics. 67, p. 218-224Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Assignment of Genes Coding for Brown Eye Colour (BEY2) and Brown Hair colour (HCL3) on Chromosome 15q
Eiberg, Hans Rudolf Lytchoff & Mohr, J., 1996, In: European Journal of Human Genetics. 4, p. 237-241Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Dombrock blood group (DO): assignment to chromosome 12p
Eiberg, Hans Rudolf Lytchoff & Mohr, J., 1996, In: Human Genetics. 98, p. 518-521Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Dominant optic atrophy mapped to chromosome 3q region
Kjer, B., Eiberg, Hans Rudolf Lytchoff, Kjer, P. & Rosenberg, T., 1996, In: Acta Ophthalmologica Scandinavica. 74, p. 3-7Research 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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1887
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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 -
408
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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