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Browsing by Author Brinke, H. te

Full Text	Issue Date	Title	Author(s)
	2007	Development of a genotyping microarray for Usher syndrome.	Cremers, F.P.M.; Kimberling, W.J.; Kulm, M.; Brouwer, A.P.M. de; Wijk, E. van, 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	Phenotype determination guides swift genotyping of a DFNA2/KCNQ4 family with a hot spot mutation (W276S).	Topsakal, V.; Pennings, R.J.E.; Brinke, H. te; Hamel, B.C.J.; Huygen, P.L.M., et al
	2005	Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2.	Reiners, J.; Wijk, E. van; Marker, T.; Zimmermann, U.; Jurgens, K., et al
	2004	Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II.	Wijk, E. van; Pennings, R.J.E.; Brinke, H. te; Claassen, A.M.W.; Yntema, H.G., et al
	2004	USH2A mutation analysis in 70 Dutch families with Usher syndrome type II.	Pennings, R.J.E.; Brinke, H. te; Weston, M.D.; Claassen, A.M.W.; Orten, D.J., et al