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

Sarah B Emery

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 28, 2009
Otosclerosis or congenital stapes ankylosis? The diagnostic role of genetic analysisSarah B Emery, Anna Meyer, Laura Miller, et al.
Nucleic Acids Research|October 29, 2014
The genomic landscape of polymorphic human nuclear mitochondrial insertionsGargi Dayama, Sarah B Emery, Jeffrey M Kidd, et al.
Ophthalmic Genetics|November 12, 2010
Congenital cataracts in two siblings with Wolfram syndromeRebecca B Mets, Sarah B Emery, Marci M Lesperance, et al.
Genome Biology and Evolution|July 1, 2016
Y-Chromosome Structural Diversity in the Bonobo and Chimpanzee LineagesMatthew T Oetjens, Feichen Shen, Sarah B Emery, et al.
Genome Biology|June 12, 2016
Resolving complex structural genomic rearrangements using a randomized approachXuefang Zhao, Sarah B Emery, Bridget Myers, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 1, 2014
CHD7 mutations and CHARGE syndrome in semicircular canal dysplasiaGlenn E Green, Farhan S Huq, Sarah B Emery, et al.
Archives of Otolaryngology--Head & Neck Surgery|January 19, 2011
Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 geneJameson Arnett, Sarah B Emery, Theresa B Kim, et al.
Nucleic Acids Research|December 20, 2019
Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technologyWeichen Zhou, Sarah B Emery, Diane A Flasch, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 14, 2010
Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in DrosophilaCynthia J Schoen, Sarah B Emery, Marc C Thorne, et al.
Biorxiv : the Preprint Server for Biology|March 22, 2023
Mapping the Complex Genetic Landscape of Human NeuronsChen Sun, Kunal Kathuria, Sarah B Emery, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 28, 2009
Otosclerosis or congenital stapes ankylosis? The diagnostic role of genetic analysisSarah B Emery, Anna Meyer, Laura Miller, et al.
Nucleic Acids Research|October 29, 2014
The genomic landscape of polymorphic human nuclear mitochondrial insertionsGargi Dayama, Sarah B Emery, Jeffrey M Kidd, et al.
Ophthalmic Genetics|November 12, 2010
Congenital cataracts in two siblings with Wolfram syndromeRebecca B Mets, Sarah B Emery, Marci M Lesperance, et al.
Genome Biology and Evolution|July 1, 2016
Y-Chromosome Structural Diversity in the Bonobo and Chimpanzee LineagesMatthew T Oetjens, Feichen Shen, Sarah B Emery, et al.
Genome Biology|June 12, 2016
Resolving complex structural genomic rearrangements using a randomized approachXuefang Zhao, Sarah B Emery, Bridget Myers, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 1, 2014
CHD7 mutations and CHARGE syndrome in semicircular canal dysplasiaGlenn E Green, Farhan S Huq, Sarah B Emery, et al.
Archives of Otolaryngology--Head & Neck Surgery|January 19, 2011
Autosomal dominant progressive sensorineural hearing loss due to a novel mutation in the KCNQ4 geneJameson Arnett, Sarah B Emery, Theresa B Kim, et al.
Nucleic Acids Research|December 20, 2019
Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technologyWeichen Zhou, Sarah B Emery, Diane A Flasch, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 14, 2010
Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in DrosophilaCynthia J Schoen, Sarah B Emery, Marc C Thorne, et al.
Biorxiv : the Preprint Server for Biology|March 22, 2023
Mapping the Complex Genetic Landscape of Human NeuronsChen Sun, Kunal Kathuria, Sarah B Emery, et al.
Pageof 2