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Browsing by Author Zwaag, B. van der

Full Text	Issue Date	Title	Author(s)
	2011	Social Responsiveness Scale-aided analysis of the clinical impact of copy number variations in autism.	Daalen, E. van; Kemner, C.; Verbeek, N.E.; Zwaag, B. van der; Dijkhuizen, T., et al
	2010	Association of whirlin with Cav1.3 (alpha1D) channels in photoreceptors, defining a novel member of the usher protein network.	Kersten, F.F.J.; Wijk, E. van; Reeuwijk, J. van; Zwaag, B. van der; Marker, T., et al
	2010	Disruption of the podosome adaptor protein TKS4 (SH3PXD2B) causes the skeletal dysplasia, eye, and cardiac abnormalities of Frank-Ter Haar Syndrome.	Iqbal, Z.; Cejudo-Martin, P.; Brouwer, A.; Zwaag, B. van der; Ruiz-Lozano, P., et al
	2008	Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.	Ahmed, Z.M.; Masmoudi, S.; Kalay, E.; Belyantseva, I.A.; Mosrati, M.A., et al
	2008	Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.	Collin, R.W.J.; Kalay, E.; Tariq, M.; Peters, T.A.; Zwaag, B. van der, et al
	2007	Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.	Hollander, A.I. den; Koenekoop, R.K.; Mohamed, M.D.; Arts, H.H.; Boldt, K., et al
	2007	MPP1 links the Usher protein network and the Crumbs protein complex in the retina.	Gosens, I.; Wijk, E. van; Kersten, F.F.J.; Krieger, E.; Zwaag, B. van der, et al
	2007	MPP1 links the Usher protein network and the Crumbs protein complex in the retina.	Gosens, I.; Wijk, E. van; Kersten, F.F.J.; Krieger, E.; Zwaag, B. van der, et al
	2006	The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1.	Wijk, E. van; Zwaag, B. van der; Peters, T.A.; Zimmermann, U.; Brinke, H. te, et al
	2005	Plexin D1 expression is induced on tumor vasculature and tumor cells: a novel target for diagnosis and therapy?	Roodink, I.; Raats, J.M.H.; Zwaag, B. van der; Verrijp, K.; Kusters, B., et al
	2005	Identifying new candidate genes for hereditary facial paresis on chromosome 3q21-q22 by RNA in situ hybridization in mouse.	Zwaag, B. van der; Burbach, J.P.; Scharfe, C.; Oefner, P.J.; Brunner, H.G., et al
	2005	Plexin D1 expression is induced on tumor vasculature and tumor cells: a novel target for diagnosis and therapy?	Roodink, I.; Raats, J.M.H.; Zwaag, B. van der; Verrijp, K.; Kusters, B., et al
	2005	Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis.	Zwaag, B. van der; Burbach, J.P.; Brunner, H.G.; Bokhoven, J.H.L.M. van; Padberg, G.W.A.M.
	2005	The neuropathology of hereditary congenital facial palsy vs Mobius syndrome.	Verzijl, H.T.F.M.; Zwaag, B. van der; Lammens, M.M.Y.; Donkelaar, H.J. ten; Padberg, G.W.A.M.
	2004	Sequence analysis of the PLEXIN-D1 gene in Mobius syndrome patients.	Zwaag, B. van der; Verzijl, H.T.F.M.; Wichers, K.H.; Beltran Valero de Bernabe, D.; Brunner, H.G., et al