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

Anneke I. den Hollander

Department of Human Genetics

University Hospital Nijmegen

Netherlands

[email]@antrg.azn.nl

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Human Genetics, University Hospital Nijmegen, Netherlands. 1999 - 2002
  • Department of Human Genetics, University Medical Centre Nijmegen, Geert Grooteplein 10, 6500 HB Nijmegen, Netherlands. 2001

References

  1. Isolation of Crb1, a mouse homologue of Drosophila crumbs, and analysis of its expression pattern in eye and brain. den Hollander, A.I., Ghiani, M., de Kok, Y.J., Wijnholds, J., Ballabio, A., Cremers, F.P., Broccoli, V. Mech. Dev. (2002) [Pubmed]
  2. Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene. den Hollander, A.I., Heckenlively, J.R., van den Born, L.I., de Kok, Y.J., van der Velde-Visser, S.D., Kellner, U., Jurklies, B., van Schooneveld, M.J., Blankenagel, A., Rohrschneider, K., Wissinger, B., Cruysberg, J.R., Deutman, A.F., Brunner, H.G., Apfelstedt-Sylla, E., Hoyng, C.B., Cremers, F.P. Am. J. Hum. Genet. (2001) [Pubmed]
  3. CRB1 has a cytoplasmic domain that is functionally conserved between human and Drosophila. den Hollander, A.I., Johnson, K., de Kok, Y.J., Klebes, A., Brunner, H.G., Knust, E., Cremers, F.P. Hum. Mol. Genet. (2001) [Pubmed]
  4. Refined mapping of the gene for autosomal dominant retinitis pigmentosa (RP17) on chromosome 17q22. den Hollander, A.I., van der Velde-Visser, S.D., Pinckers, A.J., Hoyng, C.B., Brunner, H.G., Cremers, F.P. Hum. Genet. (1999) [Pubmed]
  5. Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridization. den Hollander, A.I., van Driel, M.A., de Kok, Y.J., van de Pol, D.J., Hoyng, C.B., Brunner, H.G., Deutman, A.F., Cremers, F.P. Genomics (1999) [Pubmed]
 
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