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Browsing by Author Sikkema-Raddatz, B.

Full Text	Issue Date	Title	Author(s)
	2012	Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies	Nowakowska, B.A.; de Leeuw, N.; Ruivenkamp, C.A.; Sikkema-Raddatz, B.; Crolla, J.A., et al
	2012	Genome-wide arrays in routine diagnostics of hematological malignancies	Simons, A.; Sikkema-Raddatz, B.; de Leeuw, N.; Konrad, N.C.; Hastings, R.J., et al
	2011	Balanced into array: genome-wide array analysis in 54 patients with an apparently balanced de novo chromosome rearrangement and a meta-analysis	Feenstra, I.; Hanemaaijer, N.; Sikkema-Raddatz, B.; Yntema, H.G.; Dijkhuizen, T., et al
	2010	Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.	Willemsen, M.H.; Fernandez, B.A.; Bacino, C.A.; Gerkes, E.; Brouwer, A.P.M. de, et al
	2009	Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.	Bijlsma, E.K.; Gijsbers, A.C.; Schuurs-Hoeijmakers, J.H.M.; Haeringen, A. van; Fransen van de Putte, D.E., 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
	2006	An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell cultures.	Sikkema-Raddatz, B.; Suijkerbuijk, R.F.; Vlag, J. van der; Stoepker, M.; Buys, C.H.C.M., et al