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Zippora Brownstein

Showing results (11-20 of 30) with videos related to

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Genetic Testing and Molecular Biomarkers|December 26, 2013
The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestryDoron M Behar, Bella Davidov, Zippora Brownstein, et al.
Archives of Otolaryngology--Head & Neck Surgery|May 17, 2006
Connexin-associated deafness and speech perception outcome of cochlear implantationRiki Taitelbaum-Swead, Zippora Brownstein, Chava Muchnik, et al.
European Journal of Human Genetics : EJHG|October 10, 2013
Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencingZippora Brownstein, Amal Abu-Rayyan, Daphne Karfunkel-Doron, et al.
Annals of Human Genetics|August 10, 2021
PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern IndiaParidhy Vanniya S, Jayasankaran Chandru, Justin Margret Jeffrey, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 28, 2021
Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum DisorderRyan J Carlson, Alicia Quesnel, Dawson Wells, et al.
Nucleic Acids Research|November 25, 2010
SPIKE: a database of highly curated human signaling pathwaysArnon Paz, Zippora Brownstein, Yaara Ber, et al.
Human Genomics|October 7, 2025
A multicenter study reveals a novel pathogenic splice-site founder variant in OTOFZippora Brownstein, Lara Kamal, Shir Mishan-Montefiori, et al.
Pediatric Research|March 19, 2004
The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosaZippora Brownstein, Tamar Ben-Yosef, Orit Dagan, et al.
European Journal of Human Genetics : EJHG|August 25, 2018
Genetics of hearing loss in the Arab population of Northern IsraelNada Danial-Farran, Zippora Brownstein, Suleyman Gulsuner, et al.
Human Mutation|April 23, 2013
Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and miceThomas Parzefall, Shaked Shivatzki, Danielle R Lenz, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Genetic Testing and Molecular Biomarkers|December 26, 2013
The many faces of sensorineural hearing loss: one founder and two novel mutations affecting one family of mixed Jewish ancestryDoron M Behar, Bella Davidov, Zippora Brownstein, et al.
Archives of Otolaryngology--Head & Neck Surgery|May 17, 2006
Connexin-associated deafness and speech perception outcome of cochlear implantationRiki Taitelbaum-Swead, Zippora Brownstein, Chava Muchnik, et al.
European Journal of Human Genetics : EJHG|October 10, 2013
Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencingZippora Brownstein, Amal Abu-Rayyan, Daphne Karfunkel-Doron, et al.
Annals of Human Genetics|August 10, 2021
PNPT1, MYO15A, PTPRQ, and SLC12A2-associated genetic and phenotypic heterogeneity among hearing impaired assortative mating families in Southern IndiaParidhy Vanniya S, Jayasankaran Chandru, Justin Margret Jeffrey, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 28, 2021
Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum DisorderRyan J Carlson, Alicia Quesnel, Dawson Wells, et al.
Nucleic Acids Research|November 25, 2010
SPIKE: a database of highly curated human signaling pathwaysArnon Paz, Zippora Brownstein, Yaara Ber, et al.
Human Genomics|October 7, 2025
A multicenter study reveals a novel pathogenic splice-site founder variant in OTOFZippora Brownstein, Lara Kamal, Shir Mishan-Montefiori, et al.
Pediatric Research|March 19, 2004
The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosaZippora Brownstein, Tamar Ben-Yosef, Orit Dagan, et al.
European Journal of Human Genetics : EJHG|August 25, 2018
Genetics of hearing loss in the Arab population of Northern IsraelNada Danial-Farran, Zippora Brownstein, Suleyman Gulsuner, et al.
Human Mutation|April 23, 2013
Cytoplasmic mislocalization of POU3F4 due to novel mutations leads to deafness in humans and miceThomas Parzefall, Shaked Shivatzki, Danielle R Lenz, et al.
Pageof 3