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

Crystel Bonnet

Showing results (31-40 of 72) with videos related to

Pageof 8
Sort By:
Gene|March 20, 2018
A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan familySara Salime, Zied Riahi, Soukaina Elrharchi, et al.
BMC Cancer|July 20, 2022
Screening of BRCA1/2 variants in Mauritanian breast cancer patientsSelma Mohamed Brahim, Ekht Elbenina Zein, Crystel Bonnet, et al.
Biochemical and Biophysical Research Communications|March 17, 2010
Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever!Sandrine Marlin, Delphine Feldmann, Yann Nguyen, et al.
International Journal of Pediatric Otorhinolaryngology|July 17, 2013
Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcomeZied Riahi, Rim Zainine, Yosra Mellouli, et al.
International Journal of Pediatric Otorhinolaryngology|July 30, 2018
Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa provinceSonia Talbi, Crystel Bonnet, Zied Riahi, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencingFatima Ammar-Khodja, Crystel Bonnet, Malika Dahmani, et al.
International Journal of Pediatric Otorhinolaryngology|July 3, 2016
A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian familyAsma Behlouli, Crystel Bonnet, Samia Abdi, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|March 17, 2023
Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafnessMalak Salame, Crystel Bonnet, Ely Cheikh Mohamed Moctar, et al.
Eye (London, England)|July 20, 2019
Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A geneOlaia Subirà, Jaume Català-Mora, Jesús Díaz-Cascajosa, et al.
BMC Infectious Diseases|June 21, 2024
Genetic variation of TLR3 gene is associated with the outcome of hepatitis b infection in mauritanian patients: case control studyTetou Soumbara, Crystel Bonnet, Cheikh Tijani Hamed, et al.
Pageof 8

Showing results (31-40 of 72) with videos related to

Sort By:
Pageof 8
Gene|March 20, 2018
A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan familySara Salime, Zied Riahi, Soukaina Elrharchi, et al.
BMC Cancer|July 20, 2022
Screening of BRCA1/2 variants in Mauritanian breast cancer patientsSelma Mohamed Brahim, Ekht Elbenina Zein, Crystel Bonnet, et al.
Biochemical and Biophysical Research Communications|March 17, 2010
Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever!Sandrine Marlin, Delphine Feldmann, Yann Nguyen, et al.
International Journal of Pediatric Otorhinolaryngology|July 17, 2013
Compound heterozygosity for dominant and recessive GJB2 mutations in a Tunisian family and association with successful cochlear implant outcomeZied Riahi, Rim Zainine, Yosra Mellouli, et al.
International Journal of Pediatric Otorhinolaryngology|July 30, 2018
Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa provinceSonia Talbi, Crystel Bonnet, Zied Riahi, et al.
Molecular Genetics & Genomic Medicine|June 2, 2015
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencingFatima Ammar-Khodja, Crystel Bonnet, Malika Dahmani, et al.
International Journal of Pediatric Otorhinolaryngology|July 3, 2016
A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian familyAsma Behlouli, Crystel Bonnet, Samia Abdi, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|March 17, 2023
Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafnessMalak Salame, Crystel Bonnet, Ely Cheikh Mohamed Moctar, et al.
Eye (London, England)|July 20, 2019
Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A geneOlaia Subirà, Jaume Català-Mora, Jesús Díaz-Cascajosa, et al.
BMC Infectious Diseases|June 21, 2024
Genetic variation of TLR3 gene is associated with the outcome of hepatitis b infection in mauritanian patients: case control studyTetou Soumbara, Crystel Bonnet, Cheikh Tijani Hamed, et al.
Pageof 8