Guy Van Camp
Department of Medical Genetics
University of Antwerp-UIA
Antwerp
Belgium
Name/email consistency: high
- Genetics of microtia and associated syndromes. Alasti, F., Van Camp, G. J. Med. Genet. (2009)
- A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene. Van Camp, G., Snoeckx, R.L., Hilgert, N., van den Ende, J., Fukuoka, H., Wagatsuma, M., Suzuki, H., Smets, R.M., Vanhoenacker, F., Declau, F., Van de Heyning, P., Usami, S. Am. J. Hum. Genet. (2006)
- A mutational hot spot in the KCNQ4 gene responsible for autosomal dominant hearing impairment. Van Camp, G., Coucke, P.J., Akita, J., Fransen, E., Abe, S., De Leenheer, E.M., Huygen, P.L., Cremers, C.W., Usami, S. Hum. Mutat. (2002)