|
|
DSpace at RU >
Browsing by Author Rooms, L.
Showing results 1 to 5 of 5
| Full Text | Issue Date | Title | Author(s) | | 2009 | Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome. | Aa, N. van der; Rooms, L.; Weyer, G. van de; Ende, J.J. van den; Reyniers, E., et al |
| 2008 | Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. | Koolen, D.A.; Sharp, A.J.; Hurst, J.A.; Firth, H.V.; Knight, S.J., et al |
| 2008 | Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis. | Bon, B.W.M. van; Koolen, D.A.; Borgatti, R.; Magee, A.; Garcia-Minaur, S., et al |
| 2008 | Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches. | Koolen, D.A.; Sistermans, E.A.; Nilessen, W.; Knight, S.J.; Regan, R., et al |
| 2007 | Dandy-Walker complex in a boy with a 5 Mb deletion of region 1q44 due to a paternal t(1;20)(q44;q13.33). | Poot, M.; Kroes, H.Y.; Wijst, S.E. van der; Eleveld, M.J.; Rooms, L., et al |
Showing results 1 to 5 of 5
|