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Browsing by Author Bitner-Glindzicz, M.

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
	2005	GJB2 mutations and degree of hearing loss: a multicenter study.	Snoeckx, R.L.; Huygen, P.L.M.; Feldmann, D.; Marlin, S.; Denoyelle, F., et al
	1996	Identification of a hot spot for microdeletions in patients with X-linked deafness type 3 (DFN3) 900 kb proximal to the DFN3 gene POU3F4	Kok, Y.J.M. de; Vossenaar, E.R.; Cremers, C.W.R.J.; Dahl, N.; Laporte, J., et al
	1995	Mapping and cloning hereditary deafness genes	Cremers, F.P.M.; Bitner-Glindzicz, M.; Pembrey, M.E.; Ropers, H.H.
	1995	Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4	Kok, Y.J.M. de; Maarel, S.M. van der; Bitner-Glindzicz, M.; Huber-Bach, I.; Monaco, A.P., et al
	1995	Further mutations in Brain 4 (POU3F4) clarify the phenotype in the X-linked deafness, DFN3	Bitner-Glindzicz, M.; Turnpenny, P.; Höglund, P.; Kääriäinen, H.; Sankila, E.M., et al