Similar gene expression profiles of sporadic, PGL2-, and SDHD-linked paragangliomas suggest a common pathway to tumorigenesis

por Hensen, Erik F, Goeman, Jelle J, Oosting, Jan, Van der Mey, Andel GL, Hogendoorn, Pancras CW, Cremers, Cor WRJ, Devilee, Peter, Cornelisse, Cees J
Publicado 2009

Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1

por Hogewind, Barend F.T., Pennings, Ronald J.E., Hol, Frans A., Kunst, Henricus P.M., Hoefsloot, Elisabeth H., Cruysberg, Johannes R.M., Cremers, Cor W.R.J.
Publicado 2010

Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype

por Swinnen, Freya KR, Coucke, Paul J, De Paepe, Anne M, Symoens, Sofie, Malfait, Fransiska, Gentile, Filomena V, Sangiorgi, Luca, D'Eufemia, Patrizia, Celli, Mauro, Garretsen, Ton JTM, Cremers, Cor WRJ, Dhooge, Ingeborg JM, De Leenheer, Els MR
Publicado 2011