C W Cremers|S J Geerts - JoVE Visualize

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Human Mutation|April 24, 2001

Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness familiesZ H Shah, M Toompuu, T Hakkinen, et al.

American Journal of Human Genetics|July 1, 1992

Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)I Bach, H G Brunner, P Beighton, et al.

Genomics|February 15, 1997

The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7qP Coucke, G Van Camp, O Demirhan, et al.

Genomics|January 15, 1994

Mapping of the choroideremia-like (CHML) gene at 1q42-qter and mutation analysis in patients with Usher syndrome type IIH von Bokhoven, C von Genderen, C M Molloy, 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.

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.

Otolaryngologic Clinics of North America|May 31, 2001

Multicenter audiometric results with the Vibrant Soundbridge, a semi-implantable hearing device for sensorineural hearing impairmentA F Snik, E A Mylanus, C W Cremers, 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.

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Showing results (141-150 of 158) with videos related to

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Pageof 16

Human Mutation|April 24, 2001

Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness familiesZ H Shah, M Toompuu, T Hakkinen, et al.

American Journal of Human Genetics|July 1, 1992

Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)I Bach, H G Brunner, P Beighton, et al.

Genomics|February 15, 1997

The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7qP Coucke, G Van Camp, O Demirhan, et al.

Genomics|January 15, 1994

Mapping of the choroideremia-like (CHML) gene at 1q42-qter and mutation analysis in patients with Usher syndrome type IIH von Bokhoven, C von Genderen, C M Molloy, 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.

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.

Otolaryngologic Clinics of North America|May 31, 2001

Multicenter audiometric results with the Vibrant Soundbridge, a semi-implantable hearing device for sensorineural hearing impairmentA F Snik, E A Mylanus, C W Cremers, 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.

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