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Hans-Henrik M Dahl

Showing results (1-10 of 41) with videos related to

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Journal of the Association for Research in Otolaryngology : JARO|June 20, 2002
In silico analyses of mouse inner-ear transcriptsTuomas Klockars, Teemu Perheentupa, Hans-Henrik M Dahl
Genetic Testing and Molecular Biomarkers|March 4, 2011
Identification of SLC26A4 mutations in patients with hearing loss and enlarged vestibular aqueduct using high-resolution melting curve analysisStephen Mercer, Patricia Mutton, Hans-Henrik M Dahl
Journal of the Neurological Sciences|August 7, 2002
Clinical and molecular features of adPEO due to mutations in the Twinkle geneSharon Lewis, Wendy Hutchison, Dominic Thyagarajan, et al.
American Journal of Medical Genetics. Part A|August 30, 2007
Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28David J Amor, Hans-Henrik M Dahl, Melanie Bahlo, et al.
The American Journal of Pathology|February 15, 2012
Identification of three novel hearing loss mouse strains with mutations in the Tmc1 geneShehnaaz S M Manji, Kerry A Miller, Louise H Williams, et al.
Hearing Research|March 15, 2013
Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunctionLouise H Williams, Kerry A Miller, Hans-Henrik M Dahl, et al.
Plos One|October 3, 2013
Eeyore: a novel mouse model of hereditary deafnessKerry A Miller, Louise H Williams, Hans-Henrik M Dahl, et al.
Audiology & Neuro-Otology|August 9, 2003
Language and speech perception outcomes in hearing-impaired children with and without connexin 26 mutationsHans-Henrik M Dahl, Melissa Wake, Julia Sarant, et al.
Journal of Neuroscience Research|December 13, 2005
Molecular characterization and expression of maternally expressed gene 3 (Meg3/Gtl2) RNA in the mouse inner earShehnaaz S M Manji, Brita S Sørensen, Tuomas Klockars, et al.
Plos One|April 5, 2013
Etiology and audiological outcomes at 3 years for 364 children in AustraliaHans-Henrik M Dahl, Teresa Y C Ching, Wendy Hutchison, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Journal of the Association for Research in Otolaryngology : JARO|June 20, 2002
In silico analyses of mouse inner-ear transcriptsTuomas Klockars, Teemu Perheentupa, Hans-Henrik M Dahl
Genetic Testing and Molecular Biomarkers|March 4, 2011
Identification of SLC26A4 mutations in patients with hearing loss and enlarged vestibular aqueduct using high-resolution melting curve analysisStephen Mercer, Patricia Mutton, Hans-Henrik M Dahl
Journal of the Neurological Sciences|August 7, 2002
Clinical and molecular features of adPEO due to mutations in the Twinkle geneSharon Lewis, Wendy Hutchison, Dominic Thyagarajan, et al.
American Journal of Medical Genetics. Part A|August 30, 2007
Keipert syndrome (Nasodigitoacoustic syndrome) is X-linked and maps to Xq22.2-Xq28David J Amor, Hans-Henrik M Dahl, Melanie Bahlo, et al.
The American Journal of Pathology|February 15, 2012
Identification of three novel hearing loss mouse strains with mutations in the Tmc1 geneShehnaaz S M Manji, Kerry A Miller, Louise H Williams, et al.
Hearing Research|March 15, 2013
Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunctionLouise H Williams, Kerry A Miller, Hans-Henrik M Dahl, et al.
Plos One|October 3, 2013
Eeyore: a novel mouse model of hereditary deafnessKerry A Miller, Louise H Williams, Hans-Henrik M Dahl, et al.
Audiology & Neuro-Otology|August 9, 2003
Language and speech perception outcomes in hearing-impaired children with and without connexin 26 mutationsHans-Henrik M Dahl, Melissa Wake, Julia Sarant, et al.
Journal of Neuroscience Research|December 13, 2005
Molecular characterization and expression of maternally expressed gene 3 (Meg3/Gtl2) RNA in the mouse inner earShehnaaz S M Manji, Brita S Sørensen, Tuomas Klockars, et al.
Plos One|April 5, 2013
Etiology and audiological outcomes at 3 years for 364 children in AustraliaHans-Henrik M Dahl, Teresa Y C Ching, Wendy Hutchison, et al.
Pageof 5