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Browsing by Author Hildebrand, M.S.

Full Text	Issue Date	Title	Author(s)
	2011	Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human	Charizopoulou, N.; Lelli, A.; Schraders, M.; Ray, K.; Hildebrand, M.S., et al
	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
	2010	Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population.	Hildebrand, M.S.; Kahrizi, K.; Bromhead, C.J.; Shearer, A.E.; Webster, J.A., et al
	2010	A novel mutation in COCH-implications for genotype-phenotype correlations in DFNA9 hearing loss.	Hildebrand, M.S.; Gandolfo, L.; Shearer, A.E.; Webster, J.A.; Jensen, M., et al
	2009	A contemporary review of AudioGene audioprofiling: a machine-based candidate gene prediction tool for autosomal dominant nonsyndromic hearing loss.	Hildebrand, M.S.; DeLuca, A.; Taylor, K.R.; Hoskinson, D.P.; Hur, I.A., et al
	2008	Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus.	Hildebrand, M.S.; Tack, D.; McMordie, S.J.; DeLuca, A.; Hur, I.A., et al