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F Declau

Showing results (21-30 of 32) with videos related to

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International Journal of Pediatric Otorhinolaryngology|March 22, 2008
Case report: "auditory neuropathy" in a newborn caused by a cerebellopontine angle arachnoid cystA N Boudewyns, F Declau, D De Ridder, et al.
Human Molecular Genetics|February 13, 2001
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locusS Wayne, N G Robertson, F DeClau, 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.
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.
Nature Genetics|March 18, 1999
Deafness linked to DFNA2: one locus but how many genes?P Van Hauwe, P J Coucke, F Declau, 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.
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.
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.
Genomics|April 1, 1997
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.
Journal of Medical Genetics|May 19, 2001
A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutationE Fransen, M Verstreken, S J Bom, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
International Journal of Pediatric Otorhinolaryngology|March 22, 2008
Case report: "auditory neuropathy" in a newborn caused by a cerebellopontine angle arachnoid cystA N Boudewyns, F Declau, D De Ridder, et al.
Human Molecular Genetics|February 13, 2001
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locusS Wayne, N G Robertson, F DeClau, 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.
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.
Nature Genetics|March 18, 1999
Deafness linked to DFNA2: one locus but how many genes?P Van Hauwe, P J Coucke, F Declau, 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.
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.
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.
Genomics|April 1, 1997
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1pG Van Camp, P J Coucke, H Kunst, et al.
Journal of Medical Genetics|May 19, 2001
A common ancestor for COCH related cochleovestibular (DFNA9) patients in Belgium and The Netherlands bearing the P51S mutationE Fransen, M Verstreken, S J Bom, et al.
Pageof 4