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Markus Pfister

Showing results (51-60 of 57) with videos related to

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Molecular Genetics & Genomic Medicine|September 26, 2017
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and <i>PEX26</i> mutated in Heimler syndromeChristine Neuhaus, Tobias Eisenberger, Christian Decker, et al.
American Journal of Human Genetics|September 2, 2008
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment traitJeroen R Huyghe, Lut Van Laer, Jan-Jaap Hendrickx, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 3, 2007
The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing lossEls Van Eyken, Lut Van Laer, Erik Fransen, et al.
Human Molecular Genetics|December 3, 2008
GRM7 variants confer susceptibility to age-related hearing impairmentRick A Friedman, Lut Van Laer, Matthew J Huentelman, et al.
Human Molecular Genetics|October 9, 2007
The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairmentLut Van Laer, Els Van Eyken, Erik Fransen, et al.
Journal of the Association for Research in Otolaryngology : JARO|June 11, 2008
Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter studyErik Fransen, Vedat Topsakal, Jan-Jaap Hendrickx, et al.
American Journal of Human Genetics|December 29, 2005
GJB2 mutations and degree of hearing loss: a multicenter studyRikkert L Snoeckx, Patrick L M Huygen, Delphine Feldmann, et al.
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Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Molecular Genetics & Genomic Medicine|September 26, 2017
Next-generation sequencing reveals the mutational landscape of clinically diagnosed Usher syndrome: copy number variations, phenocopies, a predominant target for translational read-through, and <i>PEX26</i> mutated in Heimler syndromeChristine Neuhaus, Tobias Eisenberger, Christian Decker, et al.
American Journal of Human Genetics|September 2, 2008
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment traitJeroen R Huyghe, Lut Van Laer, Jan-Jaap Hendrickx, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 3, 2007
The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing lossEls Van Eyken, Lut Van Laer, Erik Fransen, et al.
Human Molecular Genetics|December 3, 2008
GRM7 variants confer susceptibility to age-related hearing impairmentRick A Friedman, Lut Van Laer, Matthew J Huentelman, et al.
Human Molecular Genetics|October 9, 2007
The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairmentLut Van Laer, Els Van Eyken, Erik Fransen, et al.
Journal of the Association for Research in Otolaryngology : JARO|June 11, 2008
Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter studyErik Fransen, Vedat Topsakal, Jan-Jaap Hendrickx, et al.
American Journal of Human Genetics|December 29, 2005
GJB2 mutations and degree of hearing loss: a multicenter studyRikkert L Snoeckx, Patrick L M Huygen, Delphine Feldmann, et al.
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