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Showing results (41-50 of 49) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 8, 2001
A Two-stage bipodal screening model for universal neonatal hearing screeningP J Govaerts, M Yperman, G De Ceulaer, et al.
Acta Oto-Rhino-Laryngologica Belgica|July 4, 1998
The LAURA Pediatric Cochlear Implant Program in Antwerp: what have we learnt in 5 years?F E Offeciers, P Govaerts, K Daemers, et al.
Journal of the American Academy of Audiology|February 8, 2021
Prediction of Behavioral T/C Levels in Cochlear Implant Patients Based Upon Analysis of Electrode ImpedancesA Zarowski, A Molisz, E Cardinael, et al.
International Journal of Pediatric Otorhinolaryngology|January 31, 2020
Influence of the pre- or postlingual status of cochlear implant recipients on behavioural T/C-levelsA Zarowski, A Molisz, L De Coninck, et al.
The American Journal of Otology|November 27, 1998
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing lossP J Govaerts, G De Ceulaer, K Daemers, et al.
American Journal of Human Genetics|February 15, 2001
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36K Van Den Bogaert, P J Govaerts, I Schatteman, et al.
American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.
Bone|April 6, 2002
Otosclerosis: a genetically heterogeneous disease involving at least three different genesK Van Den Bogaert, P J Govaerts, E M R De Leenheer, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 8, 2001
A Two-stage bipodal screening model for universal neonatal hearing screeningP J Govaerts, M Yperman, G De Ceulaer, et al.
Acta Oto-Rhino-Laryngologica Belgica|July 4, 1998
The LAURA Pediatric Cochlear Implant Program in Antwerp: what have we learnt in 5 years?F E Offeciers, P Govaerts, K Daemers, et al.
Journal of the American Academy of Audiology|February 8, 2021
Prediction of Behavioral T/C Levels in Cochlear Implant Patients Based Upon Analysis of Electrode ImpedancesA Zarowski, A Molisz, E Cardinael, et al.
International Journal of Pediatric Otorhinolaryngology|January 31, 2020
Influence of the pre- or postlingual status of cochlear implant recipients on behavioural T/C-levelsA Zarowski, A Molisz, L De Coninck, et al.
The American Journal of Otology|November 27, 1998
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing lossP J Govaerts, G De Ceulaer, K Daemers, et al.
American Journal of Human Genetics|February 15, 2001
A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36K Van Den Bogaert, P J Govaerts, I Schatteman, et al.
American Journal of Human Genetics|May 1, 1997
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24K Verhoeven, G Van Camp, P J Govaerts, et al.
Bone|April 6, 2002
Otosclerosis: a genetically heterogeneous disease involving at least three different genesK Van Den Bogaert, P J Govaerts, E M R De Leenheer, et al.
Nature Genetics|May 20, 1998
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairmentK Verhoeven, L Van Laer, K Kirschhofer, et al.
Pageof 5