Showing results (41-50 of 1,373) with videos related to
Sort By:
Pageof 138
Genomics|May 1, 1994
Linkage analysis of the whirler deafness gene on mouse chromosome 4J Fleming, M J Rogers, S D Brown, et al.Neuroscience|July 4, 2013
Pitpnm1 is expressed in hair cells during development but is not required for hearingF A Carlisle, S Pearson, K P Steel, et al.British Journal of Sports Medicine|April 30, 1998
Assessment of the flexibility of elite athletes using the modified Thomas testD HarveyActa Oto-Laryngologica|November 1, 1983
The quivering mutant mouse: hereditary deafness of central originG R Bock, M P Frank, K P Steel, et al.Archives of Otolaryngology--Head & Neck Surgery|October 1, 1992
A histologic study of nonmorphogenetic forms of hereditary hearing impairmentR J Smith, K P Steel, C Barkway, et al.Genomics|May 1, 1992
Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1K A Brown, M J Sutcliffe, K P Steel, et al.Journal of Neurocytology|October 31, 2000
Cytoskeletal integration in a highly ordered sensory epithelium in the organ of Corti: reponse to loss of cell partners in the Bronx waltzer mouseJ B Tucker, J B Mackie, T J Bussoli, et al.Genomics|March 21, 1998
Mapping of the alpha-tectorin gene (TECTA) to mouse chromosome 9 and human chromosome 11: a candidate for human autosomal dominant nonsyndromic deafnessD C Hughes, P K Legan, K P Steel, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 1, 1994
Sequencing of the olfactory marker protein gene in normal and shaker-1 mutant miceK A Brown, M J Sutcliffe, K P Steel, et al.Pageof 138