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Browsing by Author Nieuwint, A.W.
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| Full Text | Issue Date | Title | Author(s) | | 2011 | Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions | Willemsen, M.H.; Beunders, G.; Callaghan, M.; Leeuw, N. de; Nillesen, W.M., et al |
| 2009 | Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands. | Hochstenbach, R.; Binsbergen, E. van; Engelen, J.; Nieuwint, A.W.; Polstra, A., et al |
| 2008 | Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genes. | Menko, F.H.; Kneepkens, C.M.; Leeuw, N. de; Peeters, E.A.; Maldergem, L Van, et al |
Showing results 1 to 3 of 3
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