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Nederlands Tijdschrift Voor Geneeskunde|November 25, 2003
[From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)]R J Pennings, K Cryns, P L Huygen, et al.The Anatomical Record|May 23, 2000
High resolution imaging of the mouse inner ear by microtomography: a new tool in inner ear researchM P Van Spaendonck, K Cryns, P H Van De Heyning, et al.The Journal of Pharmacology and Experimental Therapeutics|October 6, 2005
Energy homeostasis and gastric emptying in ghrelin knockout miceB De Smet, I Depoortere, D Moechars, et al.Human Molecular Genetics|November 16, 2001
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing lossI N Bespalova, G Van Camp, S J Bom, et al.Journal of Medical Genetics|February 27, 2004
A genotype-phenotype correlation for GJB2 (connexin 26) deafnessK Cryns, E Orzan, A Murgia, et al.Pageof 1