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Browsing by Author Nishimura, C.J.

Full Text	Issue Date	Title	Author(s)
	2011	DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss	Hildebrand, M.S.; Morin, M.; Meyer, N.C.; Mayo, F.; Modamio-Hoybjor, S., 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