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Ahmet Mutlu

Showing results (31-40 of 37) with videos related to

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Heliyon|January 21, 2025
Pharyngeal perforations after anterior cervical spinal procedures: A systematic reviewBaha Eldin Adam, Osman Kılıç, Selma Bozcan, et al.
Audiology Research|March 24, 2026
New Insight into Potential Otoprotective Effects of Lactoferrin: Is It Paradoxically Ototoxic? An Experimental InvestigationAhmet Mutlu, Ayse Yasemin Gunduz, Burcu Bakici, et al.
American Journal of Medical Genetics. Part A|February 14, 2024
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing lossDuygu Duman, Memoona Ramzan, Asli Subasioglu, et al.
Research Square|July 1, 2024
Human Organoids for Rapid Validation of Gene Variants Linked to Cochlear MalformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
Human Genetics|January 9, 2025
Human organoids for rapid validation of gene variants linked to cochlear malformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
European Journal of Human Genetics : EJHG|February 20, 2024
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, et al.
Journal of Human Genetics|May 22, 2023
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing lossMemoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Heliyon|January 21, 2025
Pharyngeal perforations after anterior cervical spinal procedures: A systematic reviewBaha Eldin Adam, Osman Kılıç, Selma Bozcan, et al.
Audiology Research|March 24, 2026
New Insight into Potential Otoprotective Effects of Lactoferrin: Is It Paradoxically Ototoxic? An Experimental InvestigationAhmet Mutlu, Ayse Yasemin Gunduz, Burcu Bakici, et al.
American Journal of Medical Genetics. Part A|February 14, 2024
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing lossDuygu Duman, Memoona Ramzan, Asli Subasioglu, et al.
Research Square|July 1, 2024
Human Organoids for Rapid Validation of Gene Variants Linked to Cochlear MalformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
Human Genetics|January 9, 2025
Human organoids for rapid validation of gene variants linked to cochlear malformationsMohammad Faraz Zafeer, Memoona Ramzan, Duygu Duman, et al.
European Journal of Human Genetics : EJHG|February 20, 2024
Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2Memoona Ramzan, Mohammad Faraz Zafeer, Clemer Abad, et al.
Journal of Human Genetics|May 22, 2023
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing lossMemoona Ramzan, Duygu Duman, LeShon Chere Peart Hendricks, et al.
Pageof 4