Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M Verstreken

Showing results (21-30 of 33) with videos related to

Pageof 4
Sort By:
The American Journal of Otology|September 19, 2000
Audiometric analysis of a Belgian family linked to the DFNA10 locusM Verstreken, F Declau, I Schatteman, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochleaL Van Laer, G Van Camp, D van Zuijlen, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 8, 2001
Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH geneM Verstreken, F Declau, F L Wuyts, 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.
Nature Communications|October 22, 2021
StemBond hydrogels control the mechanical microenvironment for pluripotent stem cellsCéline Labouesse, Bao Xiu Tan, Chibeza C Agley, et al.
Journal of Medical Genetics|July 29, 1999
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locusG Van Camp, H Kunst, K Flothmann, et al.
Human Molecular Genetics|July 13, 1999
High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH geneE Fransen, M Verstreken, W I Verhagen, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) geneK Verhoeven, R J Ensink, V Tiranti, et al.
Nature Genetics|October 15, 1998
Nonsyndromic hearing impairment is associated with a mutation in DFNA5L Van Laer, E H Huizing, M Verstreken, 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.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
The American Journal of Otology|September 19, 2000
Audiometric analysis of a Belgian family linked to the DFNA10 locusM Verstreken, F Declau, I Schatteman, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochleaL Van Laer, G Van Camp, D van Zuijlen, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|November 8, 2001
Hereditary otovestibular dysfunction and Ménière's disease in a large Belgian family is caused by a missense mutation in the COCH geneM Verstreken, F Declau, F L Wuyts, 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.
Nature Communications|October 22, 2021
StemBond hydrogels control the mechanical microenvironment for pluripotent stem cellsCéline Labouesse, Bao Xiu Tan, Chibeza C Agley, et al.
Journal of Medical Genetics|July 29, 1999
A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locusG Van Camp, H Kunst, K Flothmann, et al.
Human Molecular Genetics|July 13, 1999
High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH geneE Fransen, M Verstreken, W I Verhagen, et al.
European Journal of Human Genetics : EJHG|March 27, 1999
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) geneK Verhoeven, R J Ensink, V Tiranti, et al.
Nature Genetics|October 15, 1998
Nonsyndromic hearing impairment is associated with a mutation in DFNA5L Van Laer, E H Huizing, M Verstreken, 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.
Pageof 4