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Browsing by Author Weegerink, N.J.D.

Full Text	Issue Date	Title	Author(s)
	2011	A new locus for otosclerosis, OTSC10, maps to chromosome 1q41-44	Schrauwen, I.; Weegerink, N.J.D.; Fransen, E.; Claes, C.; Pennings, R.J.E., et al
	2011	Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family.	Weegerink, N.J.D.; Huygen, P.L.M.; Schraders, M.; Kremer, H.; Pennings, R.J., et al
	2011	Next-generation sequencing identifies mutations of SMPX, which encodes the small muscle protein, X-linked, as a cause of progressive hearing impairment	Schraders, M.; Haas, S.A.; Weegerink, N.J.D.; Oostrik, J.; Hu, H., et al
	2011	Phenotype of the first otosclerosis family linked to OTSC10	Weegerink, N.J.D.; Schrauwen, I.; Huygen, P.L.M.; Pennings, R.J.E.; Cremers, C.W.R.J., et al
	2011	Genotype-Phenotype Correlation in DFNB8/10 Families with TMPRSS3 Mutations	Weegerink, N.J.D.; Schraders, M.; Oostrik, J.; Huygen, P.L.M.; Strom, T.M., et al
	2011	Audiometric characteristics of a Dutch family with Muckle-Wells syndrome.	Weegerink, N.J.D.; Schraders, M.; Leijendeckers, J.M.; Slieker, K.; Huygen, P.L.M., et al
	2011	Phenotypes of two Dutch DFNA3 families with mutations in GJB2	Weegerink, N.J.D.; Pennings, R.J.E.; Huygen, P.L.M.; Hoefsloot, L.H.; Cremers, C.W.R.J., et al
	2009	Allergische contactcheilitis door butylhydrosyanisol in lippenstift	Valk, J.P.; Weegerink, N.J.D.; Valk, P.G.M. van der