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Browsing by Author Leenheer, E. de

Full Text	Issue Date	Title	Author(s)
	2011	KCNQ4 K(+) channels tune mechanoreceptors for normal touch sensation in mouse and man.	Heidenreich, M.; Lechner, S.G.; Vardanyan, V.; Wetzel, C.; Cremers, C.W.R.J., et al
	2011	Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype.	Swinnen, F.K.R.; Coucke, P.J.; Paepe, A.M. De; Symoens, S.; Malfait, F., et al
	2009	Audiometric, surgical, and genetic findings in 15 ears of patients with osteogenesis imperfecta.	Swinnen, F.K.; Leenheer, E. de; Coucke, P.J.; Cremers, C.W.R.J.; Dhooge, I.J.
	2006	The phenotype of the first otosclerosis family linked to OTSC5.	Pauw, R.J.; Leenheer, E. de; Bogaert, K. van den; Huygen, P.L.M.; Camp, G. van, et al
	2005	Audiometric, vestibular, and genetic aspects of a DFNA9 family with a G88E COCH mutation.	Kemperman, M.H.; Leenheer, E. de; Huygen, P.L.M.; Duijnhoven, G.C.F. van; Morton, C., et al
	2004	Audiological characteristics of some affected members of a Dutch DFNA13/COL11A2 family.	Leenheer, E. de; Bosman, A.J.; Kunst, H.P.M.; Huygen, P.L.M.; Cremers, C.W.R.J.
	2004	A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairment.	Kemperman, M.H.; Leenheer, E. de; Huygen, P.L.M.; Wijk, E. van; Duijnhoven, G.C.F. van, et al
	2004	A novel mutation identified in the DFNA5 gene in a Dutch family: a clinical and genetic evaluation.	Bischoff, A.M.L.C.; Luijendijk, M.W.J.; Huygen, P.L.M.; Duijnhoven, G.C.F. van; Leenheer, E. de, et al
	2004	Stickler syndrome type I and Stapes ankylosis.	Baijens, L.W.; Leenheer, E. de; Weekamp, H.; Cruysberg, J.R.M.; Mortier, G.R., et al
	2004	A fifth locus for otosclerosis, OTSC5, maps to chromosome 3q22-24.	Bogaert, K. van den; Leenheer, E. de; Chen, W.; Lee, Y.; Nurnberg, P., et al