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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Thomas Rosenberg

Gordon Norrie Centre for Genetic Eye Diseases

National Eye Clinic for the Visually Impaired

Hellerup

Denmark

[email]@visaid.dk

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Affiliations

Gordon Norrie Centre for Genetic Eye Diseases, National Eye Clinic for the Visually Impaired, Hellerup, Denmark. 2003 - 2004
National Eye Clinic for the Visually Impaired, Hellerup, Denmark. 1998 - 1999

References

Variant phenotypes of incomplete achromatopsia in two cousins with GNAT2 gene mutations. Rosenberg, T., Baumann, B., Kohl, S., Zrenner, E., Jorgensen, A.L., Wissinger, B. Invest. Ophthalmol. Vis. Sci. (2004) [Pubmed]
Epidemiology of hereditary ocular disorders. Rosenberg, T. Dev. Ophthalmol (2003) [Pubmed]
Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2). Rosenberg, T., Schwahn, U., Feil, S., Berger, W. Ophthalmic Genet. (1999) [Pubmed]
X-linked ocular albinism: prevalence and mutations--a national study. Rosenberg, T., Schwartz, M. Eur. J. Hum. Genet. (1998) [Pubmed]