Geraldine R. Vink
Center for Human and Clinical Genetics
Leiden University Medical Center
Leiden
Netherlands
Name/email consistency: high
- Mutation screening of EXT1 and EXT2 by direct sequence analysis and MLPA in patients with multiple osteochondromas: splice site mutations and exonic deletions account for more than half of the mutations. Vink, G.R., White, S.J., Gabelic, S., Hogendoorn, P.C., Breuning, M.H., Bakker, E. Eur. J. Hum. Genet. (2005)