Jacqueline Schoumans
Department of Molecular Medicine and Surgery
Karolinska Institutet
Stockholm
Sweden
Name/email consistency: high
- Comprehensive mutational analysis of a cohort of Swedish Cornelia de Lange syndrome patients. Schoumans, J., Wincent, J., Barbaro, M., Djureinovic, T., Maguire, P., Forsberg, L., Staaf, J., Thuresson, A.C., Borg, A., Nordgren, A., Malm, G., Anderlid, B.M. Eur. J. Hum. Genet. (2007)
- Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2. Schoumans, J., Johansson, B., Corcoran, M., Kuchinskaya, E., Golovleva, I., Grandér, D., Forestier, E., Staaf, J., Borg, A., Gustafsson, B., Blennow, E., Nordgren, A. Br. J. Haematol. (2006)









