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Browsing by Author Rooms, L.

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Full TextIssue DateTitleAuthor(s)
2009Fourteen 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
2008Clinical 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
2008Clinical 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
2008Identification 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
2007Dandy-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
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