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Browsing by Author Nieuwint, A.W.

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Full TextIssue DateTitleAuthor(s)
2011Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletionsWillemsen, M.H.; Beunders, G.; Callaghan, M.; Leeuw, N. de; Nillesen, W.M., et al
2009Array 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
2008Variable 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
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