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Zippora Brownstein

Showing results (1-10 of 30) with videos related to

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Pediatric Research|April 25, 2009
Deafness genes in Israel: implications for diagnostics in the clinicZippora Brownstein, Karen B Avraham
Genome Biology|June 1, 2012
High-throughput sequencing to decipher the genetic heterogeneity of deafnessZippora Brownstein, Yoni Bhonker, Karen B Avraham
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
Integration of human and mouse genetics reveals pendrin function in hearing and deafnessAmiel A Dror, Zippora Brownstein, Karen B Avraham
Journal of Basic and Clinical Physiology and Pharmacology|September 6, 2013
Advances in genetic diagnostics for hereditary hearing lossNatali Idan, Zippora Brownstein, Shaked Shivatzki, et al.
Journal of Basic and Clinical Physiology and Pharmacology|August 26, 2014
Apparent phenotypic anticipation in autosomal dominant connexin 26 deafnessMeirav Sokolov, Zippora Brownstein, Moshe Frydman, et al.
Harefuah|February 13, 2020
[INNOVATIONS IN RESEARCH OF HEREDITARY DEAFNESS]Tom Ben-Dov, Zippora Brownstein, Benny Nageris, et al.
Archives of Otolaryngology--Head & Neck Surgery|April 19, 2006
Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locusZippora Brownstein, Abraham Goldfarb, Haya Levi, et al.
Journal of Clinical Medicine|October 14, 2022
Molecular Features of SLC26A4 Common Variant p.L117FArnoldas Matulevičius, Emanuele Bernardinelli, Zippora Brownstein, et al.
Fertility and Sterility|May 3, 2006
Müllerian anomalies, hearing loss, and connexin 26 mutationsJacob Rabinson, Raoul Orvieto, Amnon Shapira, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
Functional characterization of pendrin mutations found in the Israeli and Palestinian populationsSilvia Dossena, Charity Nofziger, Zippora Brownstein, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Pediatric Research|April 25, 2009
Deafness genes in Israel: implications for diagnostics in the clinicZippora Brownstein, Karen B Avraham
Genome Biology|June 1, 2012
High-throughput sequencing to decipher the genetic heterogeneity of deafnessZippora Brownstein, Yoni Bhonker, Karen B Avraham
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
Integration of human and mouse genetics reveals pendrin function in hearing and deafnessAmiel A Dror, Zippora Brownstein, Karen B Avraham
Journal of Basic and Clinical Physiology and Pharmacology|September 6, 2013
Advances in genetic diagnostics for hereditary hearing lossNatali Idan, Zippora Brownstein, Shaked Shivatzki, et al.
Journal of Basic and Clinical Physiology and Pharmacology|August 26, 2014
Apparent phenotypic anticipation in autosomal dominant connexin 26 deafnessMeirav Sokolov, Zippora Brownstein, Moshe Frydman, et al.
Harefuah|February 13, 2020
[INNOVATIONS IN RESEARCH OF HEREDITARY DEAFNESS]Tom Ben-Dov, Zippora Brownstein, Benny Nageris, et al.
Archives of Otolaryngology--Head & Neck Surgery|April 19, 2006
Chromosomal mapping and phenotypic characterization of hereditary otosclerosis linked to the OTSC4 locusZippora Brownstein, Abraham Goldfarb, Haya Levi, et al.
Journal of Clinical Medicine|October 14, 2022
Molecular Features of SLC26A4 Common Variant p.L117FArnoldas Matulevičius, Emanuele Bernardinelli, Zippora Brownstein, et al.
Fertility and Sterility|May 3, 2006
Müllerian anomalies, hearing loss, and connexin 26 mutationsJacob Rabinson, Raoul Orvieto, Amnon Shapira, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 26, 2011
Functional characterization of pendrin mutations found in the Israeli and Palestinian populationsSilvia Dossena, Charity Nofziger, Zippora Brownstein, et al.
Pageof 3