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Hela Azaiez

Showing results (1-10 of 62) with videos related to

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The Laryngoscope|June 5, 2007
In reference to temporal bone imaging in GJB2 deafnessHela Azaiez, Richard J H Smith
Biomed Research International|August 16, 2016
Advances in Molecular Genetics and the Molecular Biology of DeafnessShin-Ya Nishio, Isabelle Schrauwen, Hideaki Moteki, et al.
International Journal of Molecular Sciences|June 4, 2020
<i>DFNA5</i> (<i>GSDME</i>) c.991-15_991-13delTTC: Founder Mutation or Mutational Hotspot?Kevin T Booth, Hela Azaiez, Richard J H Smith
Journal of Medical Genetics|April 29, 2018
Old gene, new phenotype: splice-altering variants in <i>CEACAM16</i> cause recessive non-syndromic hearing impairmentKevin T Booth, Kimia Kahrizi, Hossein Najmabadi, et al.
Advanced Genetics (Hoboken, N.J.)|June 17, 2024
Unraveling the Genetic Basis of Combined Deafness and Male Infertility Phenotypes through High-Throughput Sequencing in a Unique Cohort from South IndiaJeffrey Justin Margret, Chandru Jayasankaran, Pavithra Amritkumar, et al.
Frontiers in Genetics|June 6, 2018
Intracellular Regulome Variability Along the Organ of Corti: Evidence, Approaches, Challenges, and PerspectiveKevin T Booth, Hela Azaiez, Israt Jahan, et al.
Orphanet Journal of Rare Diseases|August 23, 2012
Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle EastLilia Romdhane, Rym Kefi, Hela Azaiez, et al.
Human Genetics|August 11, 2007
Genotype-phenotype correlations for SLC26A4-related deafnessHela Azaiez, Tao Yang, Sai Prasad, et al.
Human Mutation|December 22, 2017
Exonic mutations and exon skipping: Lessons learned from DFNA5Kevin T Booth, Hela Azaiez, Kimia Kahrizi, et al.
Diagnostic Pathology|January 12, 2012
Adult Gaucher disease in southern Tunisia: report of three casesFaten Ben Rhouma, Faten Kallel, Rym Kefi, et al.
Pageof 7

Showing results (1-10 of 62) with videos related to

Sort By:
Pageof 7
The Laryngoscope|June 5, 2007
In reference to temporal bone imaging in GJB2 deafnessHela Azaiez, Richard J H Smith
Biomed Research International|August 16, 2016
Advances in Molecular Genetics and the Molecular Biology of DeafnessShin-Ya Nishio, Isabelle Schrauwen, Hideaki Moteki, et al.
International Journal of Molecular Sciences|June 4, 2020
<i>DFNA5</i> (<i>GSDME</i>) c.991-15_991-13delTTC: Founder Mutation or Mutational Hotspot?Kevin T Booth, Hela Azaiez, Richard J H Smith
Journal of Medical Genetics|April 29, 2018
Old gene, new phenotype: splice-altering variants in <i>CEACAM16</i> cause recessive non-syndromic hearing impairmentKevin T Booth, Kimia Kahrizi, Hossein Najmabadi, et al.
Advanced Genetics (Hoboken, N.J.)|June 17, 2024
Unraveling the Genetic Basis of Combined Deafness and Male Infertility Phenotypes through High-Throughput Sequencing in a Unique Cohort from South IndiaJeffrey Justin Margret, Chandru Jayasankaran, Pavithra Amritkumar, et al.
Frontiers in Genetics|June 6, 2018
Intracellular Regulome Variability Along the Organ of Corti: Evidence, Approaches, Challenges, and PerspectiveKevin T Booth, Hela Azaiez, Israt Jahan, et al.
Orphanet Journal of Rare Diseases|August 23, 2012
Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle EastLilia Romdhane, Rym Kefi, Hela Azaiez, et al.
Human Genetics|August 11, 2007
Genotype-phenotype correlations for SLC26A4-related deafnessHela Azaiez, Tao Yang, Sai Prasad, et al.
Human Mutation|December 22, 2017
Exonic mutations and exon skipping: Lessons learned from DFNA5Kevin T Booth, Hela Azaiez, Kimia Kahrizi, et al.
Diagnostic Pathology|January 12, 2012
Adult Gaucher disease in southern Tunisia: report of three casesFaten Ben Rhouma, Faten Kallel, Rym Kefi, et al.
Pageof 7