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S J Bom

Showing results (1-10 of 7) with videos related to

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British Journal of Audiology|July 13, 2000
Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypesS J Bom, H P Kunst, P L Huygen, et al.
Archives of Neurology|July 13, 2000
Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9)W I Verhagen, S J Bom, P L Huygen, et al.
Clinical Otolaryngology and Allied Sciences|February 15, 2002
Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a familyW I Verhagen, S J Bom, E Fransen, et al.
The Laryngoscope|September 28, 1999
Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9S J Bom, M H Kemperman, Y J De Kok, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 15, 2001
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCHS J Bom, E M De Leenheer, F X Lemaire, 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.
Human Molecular Genetics|February 5, 1999
A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defectsY J de Kok, S J Bom, T M Brunt, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
British Journal of Audiology|July 13, 2000
Non-syndromal autosomal dominant hearing impairment: ongoing phenotypical characterization of genotypesS J Bom, H P Kunst, P L Huygen, et al.
Archives of Neurology|July 13, 2000
Familial progressive vestibulocochlear dysfunction caused by a COCH mutation (DFNA9)W I Verhagen, S J Bom, P L Huygen, et al.
Clinical Otolaryngology and Allied Sciences|February 15, 2002
Hereditary cochleovestibular dysfunction due to a COCH gene mutation (DFNA9): a follow-up study of a familyW I Verhagen, S J Bom, E Fransen, et al.
The Laryngoscope|September 28, 1999
Progressive cochleovestibular impairment caused by a point mutation in the COCH gene at DFNA9S J Bom, M H Kemperman, Y J De Kok, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 15, 2001
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCHS J Bom, E M De Leenheer, F X Lemaire, 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.
Human Molecular Genetics|February 5, 1999
A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defectsY J de Kok, S J Bom, T M Brunt, et al.
Pageof 1