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Mustafa Tekin

Showing results (71-80 of 235) with videos related to

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Ear, Nose, & Throat Journal|October 26, 2024
Identifying DNA Variants in a Turkish Cohort with Inner Ear AnomaliesUmit Yilmaz, Müzeyyen Yildirim Baylan, Duygu Duman, et al.
Genetic Testing and Molecular Biomarkers|January 25, 2011
Mutation screening of the GJA7 (Cx45) gene in a large international series of probands with nonsyndromic hearing impairmentXiao Mei Ouyang, Denise Yan, Idil Aslan, et al.
Anatolian Journal of Cardiology|September 25, 2014
Early detection of myocardial deformation by 2D speckle tracking echocardiography in normotensive obese children and adolescentsFatih Köksal Binnetoğlu, Şule Yıldırım, Naci Topaloğlu, et al.
Scientific Reports|June 22, 2026
Losartan shows limited benefit in preclinical models of Geleophysic dysplasiaAlejo A Morales, Vladimir Camarena, LéShon Peart, 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.
International Journal of Pediatric Otorhinolaryngology|December 26, 2019
Novel OTOF pathogenic variant segregating with non-syndromic hearing loss in a consanguineous family from tribal Rajouri in Jammu and KashmirRaja A H Kuchay, Yaser Rafiq Mir, Xue Zeng, et al.
Genes|November 11, 2022
Multiple Mitochondrial Dysfunction Syndrome Type 3: A Likely Pathogenic Homozygous Variant Affecting a Patient of Cuban Descent and Literature ReviewSteven H Lang, Francesca Camponeschi, Evan de Joya, et al.
International Journal of Pediatric Otorhinolaryngology|August 22, 2012
Screening of OTOF mutations in Iran: a novel mutation and reviewNejat Mahdieh, Atefeh Shirkavand, Bahareh Rabbani, et al.
BMC Musculoskeletal Disorders|February 5, 2025
Management of extremity and pelvic fractures in earthquake: our observations and recommendationsBugra Kundakci, Akif Mirioglu, Bugra Eraslan, et al.
American Journal of Medical Genetics. Part A|April 23, 2003
Chudley-McCullough syndrome: expanded phenotype and review of the literatureKatherine Oelrich Welch, Mustafa Tekin, Walter E Nance, et al.
Pageof 24

Showing results (71-80 of 235) with videos related to

Sort By:
Pageof 24
Ear, Nose, & Throat Journal|October 26, 2024
Identifying DNA Variants in a Turkish Cohort with Inner Ear AnomaliesUmit Yilmaz, Müzeyyen Yildirim Baylan, Duygu Duman, et al.
Genetic Testing and Molecular Biomarkers|January 25, 2011
Mutation screening of the GJA7 (Cx45) gene in a large international series of probands with nonsyndromic hearing impairmentXiao Mei Ouyang, Denise Yan, Idil Aslan, et al.
Anatolian Journal of Cardiology|September 25, 2014
Early detection of myocardial deformation by 2D speckle tracking echocardiography in normotensive obese children and adolescentsFatih Köksal Binnetoğlu, Şule Yıldırım, Naci Topaloğlu, et al.
Scientific Reports|June 22, 2026
Losartan shows limited benefit in preclinical models of Geleophysic dysplasiaAlejo A Morales, Vladimir Camarena, LéShon Peart, 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.
International Journal of Pediatric Otorhinolaryngology|December 26, 2019
Novel OTOF pathogenic variant segregating with non-syndromic hearing loss in a consanguineous family from tribal Rajouri in Jammu and KashmirRaja A H Kuchay, Yaser Rafiq Mir, Xue Zeng, et al.
Genes|November 11, 2022
Multiple Mitochondrial Dysfunction Syndrome Type 3: A Likely Pathogenic Homozygous Variant Affecting a Patient of Cuban Descent and Literature ReviewSteven H Lang, Francesca Camponeschi, Evan de Joya, et al.
International Journal of Pediatric Otorhinolaryngology|August 22, 2012
Screening of OTOF mutations in Iran: a novel mutation and reviewNejat Mahdieh, Atefeh Shirkavand, Bahareh Rabbani, et al.
BMC Musculoskeletal Disorders|February 5, 2025
Management of extremity and pelvic fractures in earthquake: our observations and recommendationsBugra Kundakci, Akif Mirioglu, Bugra Eraslan, et al.
American Journal of Medical Genetics. Part A|April 23, 2003
Chudley-McCullough syndrome: expanded phenotype and review of the literatureKatherine Oelrich Welch, Mustafa Tekin, Walter E Nance, et al.
Pageof 24