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Browsing by Author Ruivenkamp, C.

Full Text	Issue Date	Title	Author(s)
	2011	Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly	Bon, B.W. van; Hoischen, A.; Hehir-Kwa, J.Y.; Brouwer, A.P. de; Ruivenkamp, C., et al
	2009	Split hand-foot malformation, tetralogy of Fallot, mental retardation and a 1 Mb 19p deletion-evidence for further heterogeneity?	Aten, E.; Hollander, N. den; Ruivenkamp, C.; Knijnenburg, J.; Bokhoven, J.H.L.M. van, 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
	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