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

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Frans P. M. Cremers

Department of Human Genetics

University Hospital Nijmegen

PO Box 9101

6500 HB Nijmegen

Netherlands

[email]@antrg.azn.nl

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Affiliation

Department of Human Genetics, University Hospital Nijmegen, PO Box 9101, 6500 HB Nijmegen, Netherlands. 1998 - 2002

References

Molecular genetics of Leber congenital amaurosis. Cremers, F.P., van den Hurk, J.A., den Hollander, A.I. Hum. Mol. Genet. (2002) [Pubmed]
The ins and outs of X-linked deafness type 3. Cremers, F.P., Cremers, C.W., Ropers, H.H. Adv. Otorhinolaryngol. (2000) [Pubmed]
Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR. Cremers, F.P., van de Pol, D.J., van Driel, M., den Hollander, A.I., van Haren, F.J., Knoers, N.V., Tijmes, N., Bergen, A.A., Rohrschneider, K., Blankenagel, A., Pinckers, A.J., Deutman, A.F., Hoyng, C.B. Hum. Mol. Genet. (1998) [Pubmed]
Genetic causes of hearing loss. Cremers, F.P. Curr. Opin. Neurol. (1998) [Pubmed]