Hans Rudolf Lytchoff Eiberg
Associate Professor
Medical Genetics Program
Blegdamsvej 3, 2200 København N.
- 2005
- Published
Mapping of Hereditary Trichilemmal Cyst (TRICY1) to Chromosome 3p24-p21.2 and Exclusion of β-CATENIN and MLH1
Eiberg, Hans Rudolf Lytchoff, Hansen, Lars, Hansen, C., Mohr, J., Teglbjærg, P. S. & Kjaer, K. W., 15 Feb 2005, In: American Journal of Medical Genetics. 133 A, 1, p. 44-47 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
A 72-year-old Danish puzzle resolved--comparative analysis of phenotypes in families with different-sized HOXD13 polyalanine expansions
Kjær, K. W., Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Utkus, A., Skovgaard, Lene Theil, Leicht, P., Opitz, J. M. & Tommerup, Niels, 2005, In: American Journal of Medical Genetics. Part A. 138, 4, p. 328-39 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Cytoplasmic expression of E-cadherin and β-Catenin correlated with LOH and hypermethylation of the APC gene in oral squamous cell carcinomas
Gao, S., Eiberg, Hans Rudolf Lytchoff, Krogdahl, A., Lui, C. & Sørensen, J. A., 2005, In: J. Oral. Pathol. Med.. Vol. 34, p. 116-119Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)
Kjær, K. W., Hansen, L., Schwabe, G. C., Marques-de-Faria, A. P., Eiberg, Hans Rudolf Lytchoff, Mundlos, S., Tommerup, Niels & Rosenberg, T., 2005, In: Journal of Medical Genetics. Vol. 42, p. 292-298Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Male-to-male transmission in Laurin-Sandrow syndrome and exclusion of RARB and RARG
Kjaer, K. W., Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Christensen, K. S., Opitz, J. M. & Tommerup, Niels, 2005, In: American Journal of Medical Genetics. Part A. 137, 2, p. 148-52 4 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified
Hansen, Lars, Eiberg, Hans Rudolf Lytchoff, Barrett, T., Bek, T., Kjærsgaard, P., Tranebjærg, Lisbeth & Rosenberg, T., 2005, In: European Journal of Human Genetics. 13, 12, p. 1275-1284Research output: Contribution to journal › Journal article › Research › peer-review
ID: 5291
Most downloads
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4547
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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
Published -
1878
downloads
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
downloads
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
Research output: Contribution to journal › Letter › Research › peer-review
Published