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Plos One
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November 13, 2015
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss
Tahir 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 Ophthalmology
Thomas Diehl, Ta Chen Peter Chang, Guney Bademci, et al.
International Journal of Pediatric Otorhinolaryngology
|
April 22, 2014
Evidence for genotype-phenotype correlation for OTOF mutations
Muzeyyen 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 orientation
Oscar Diaz-Horta, Clemer Abad, Filiz Basak Cengiz, et al.
Scientific Reports
|
October 9, 2023
Novel GPR156 variants confirm its role in moderate sensorineural hearing loss
Memoona Ramzan, Nazim Bozan, Serhat Seyhan, et al.
Clinical Case Reports
|
April 12, 2017
Dominant deafness-onychodystrophy syndrome caused by an <i>ATP6V1B2</i> mutation
Ibis 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 syndrome
Nicholas 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 TUBB3
Nicholas 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 dysfunction
Sofia Zoullas, Dayna Morel, Faraz Zafeer, et al.
Hearing Research
|
February 7, 2016
A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genes
Demet Tekin, Denise Yan, Guney Bademci, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 70) with videos related to
Sort By:
Page
of 7
Plos One
|
November 13, 2015
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss
Tahir 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 Ophthalmology
Thomas Diehl, Ta Chen Peter Chang, Guney Bademci, et al.
International Journal of Pediatric Otorhinolaryngology
|
April 22, 2014
Evidence for genotype-phenotype correlation for OTOF mutations
Muzeyyen 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 orientation
Oscar Diaz-Horta, Clemer Abad, Filiz Basak Cengiz, et al.
Scientific Reports
|
October 9, 2023
Novel GPR156 variants confirm its role in moderate sensorineural hearing loss
Memoona Ramzan, Nazim Bozan, Serhat Seyhan, et al.
Clinical Case Reports
|
April 12, 2017
Dominant deafness-onychodystrophy syndrome caused by an <i>ATP6V1B2</i> mutation
Ibis 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 syndrome
Nicholas 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 TUBB3
Nicholas 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 dysfunction
Sofia Zoullas, Dayna Morel, Faraz Zafeer, et al.
Hearing Research
|
February 7, 2016
A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genes
Demet Tekin, Denise Yan, Guney Bademci, et al.
Page
of 7