Hans Rudolf Lytchoff Eiberg
Associate Professor
Medical Genetics Program
Blegdamsvej 3, 2200 København N.
ORCID: 0000-0002-4140-1578
1 - 4 out of 4Page size: 10
- 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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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