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
- 1994
- Published
Assignment of Granular Corneal Dystrophy Groenouw Type 1 (CDGG1) to Chromosome 5q
Eiberg, Hans Rudolf Lytchoff, Møller, H. U., Brendt, I. & Mohr, J., 1994, In: European Journal of Human Genetics. 2, p. 132-138Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis
Eiberg, Hans Rudolf Lytchoff, Kjer, B., Kjer, P. & Rosenberg, T., 1994, In: Human Molecular Genetics. Vol 3, No 6, p. 977-980Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Gene for autosomale dominant congenital stationary night blindness maps to the same region as the gene for the *Gb-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3
Gal, A., Xu, S., Duvigneau, C., Schwinger, E., Piczenik, Y., Rosenberg, T. & Eiberg, Hans Rudolf Lytchoff, 1994, In: Human Molecular Genetics. Vol 3, No 2, p. 323-325Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Linkage analysis between manic depressive illness and the dopamine beta-hydroxylase gene
Ewald, H., Mors, O., Flint, T., Eiberg, Hans Rudolf Lytchoff & Kruse, T. A., 1994, In: Psychiatric Genetics. 4, p. 177-183Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Linkage analysis between manic-depressive illness and 35 classical markers
Ewald, H., Mors, O. & Eiberg, Hans Rudolf Lytchoff, 1994, In: American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics. 54, p. 144-148Research 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