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

Guney Bademci

Showing results (11-20 of 70) with videos related to

Pageof 7
Sort By:
Plos One|November 13, 2015
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing LossTahir Atik, Huseyin Onay, Ayca Aykut, et al.
American Journal of Ophthalmology|May 16, 2026
Anesthesia-Related Neurologic Risk in Patients of Venezuelan Descent: Implications for OphthalmologyThomas Diehl, Ta Chen Peter Chang, Guney Bademci, et al.
International Journal of Pediatric Otorhinolaryngology|April 22, 2014
Evidence for genotype-phenotype correlation for OTOF mutationsMuzeyyen Yildirim-Baylan, Guney Bademci, Duygu Duman, et al.
Journal of Molecular Medicine (Berlin, Germany)|October 4, 2018
Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientationOscar Diaz-Horta, Clemer Abad, Filiz Basak Cengiz, et al.
Scientific Reports|October 9, 2023
Novel GPR156 variants confirm its role in moderate sensorineural hearing lossMemoona Ramzan, Nazim Bozan, Serhat Seyhan, et al.
Clinical Case Reports|April 12, 2017
Dominant deafness-onychodystrophy syndrome caused by an <i>ATP6V1B2</i> mutationIbis Menendez, Claudia Carranza, Mariana Herrera, et al.
American Journal of Medical Genetics. Part A|January 11, 2023
Deletion of first noncoding exon in ANKRD11 leads to KBG syndromeNicholas Borja, Mohammad Faraz Zafeer, Jeimy Alfonso Rodriguez, et al.
Journal of Medical Genetics|December 6, 2024
<i>KIF21A</i>-associated peripheral neuropathy defined by impaired binding with TUBB3Nicholas A Borja, Mohammad Faraz Zafeer, Stephanie Bivona, et al.
American Journal of Medical Genetics. Part A|November 20, 2023
Two novel heterozygous exonic deletions lead to Chanarin-Dorfman syndrome in a patient with congenital ichthyosis, sensorineural hearing loss, and liver dysfunctionSofia Zoullas, Dayna Morel, Faraz Zafeer, et al.
Hearing Research|February 7, 2016
A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genesDemet Tekin, Denise Yan, Guney Bademci, et al.
Pageof 7

Showing results (11-20 of 70) with videos related to

Sort By:
Pageof 7
Plos One|November 13, 2015
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing LossTahir Atik, Huseyin Onay, Ayca Aykut, et al.
American Journal of Ophthalmology|May 16, 2026
Anesthesia-Related Neurologic Risk in Patients of Venezuelan Descent: Implications for OphthalmologyThomas Diehl, Ta Chen Peter Chang, Guney Bademci, et al.
International Journal of Pediatric Otorhinolaryngology|April 22, 2014
Evidence for genotype-phenotype correlation for OTOF mutationsMuzeyyen Yildirim-Baylan, Guney Bademci, Duygu Duman, et al.
Journal of Molecular Medicine (Berlin, Germany)|October 4, 2018
Ripor2 is involved in auditory hair cell stereociliary bundle structure and orientationOscar Diaz-Horta, Clemer Abad, Filiz Basak Cengiz, et al.
Scientific Reports|October 9, 2023
Novel GPR156 variants confirm its role in moderate sensorineural hearing lossMemoona Ramzan, Nazim Bozan, Serhat Seyhan, et al.
Clinical Case Reports|April 12, 2017
Dominant deafness-onychodystrophy syndrome caused by an <i>ATP6V1B2</i> mutationIbis Menendez, Claudia Carranza, Mariana Herrera, et al.
American Journal of Medical Genetics. Part A|January 11, 2023
Deletion of first noncoding exon in ANKRD11 leads to KBG syndromeNicholas Borja, Mohammad Faraz Zafeer, Jeimy Alfonso Rodriguez, et al.
Journal of Medical Genetics|December 6, 2024
<i>KIF21A</i>-associated peripheral neuropathy defined by impaired binding with TUBB3Nicholas A Borja, Mohammad Faraz Zafeer, Stephanie Bivona, et al.
American Journal of Medical Genetics. Part A|November 20, 2023
Two novel heterozygous exonic deletions lead to Chanarin-Dorfman syndrome in a patient with congenital ichthyosis, sensorineural hearing loss, and liver dysfunctionSofia Zoullas, Dayna Morel, Faraz Zafeer, et al.
Hearing Research|February 7, 2016
A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genesDemet Tekin, Denise Yan, Guney Bademci, et al.
Pageof 7