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

Guy Van Camp

Department of Medical Genetics

University of Antwerp-UIA

Antwerp

Belgium

[email]@ua.ac.be

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Medical Genetics, University of Antwerp-UIA, Antwerp, Belgium. 2002 - 2009

References

  1. Genetics of microtia and associated syndromes. Alasti, F., Van Camp, G. J. Med. Genet. (2009) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
 
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