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Mustafa Tekin

Showing results (1-10 of 235) with videos related to

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Balkan Medical Journal|May 3, 2024
Genetic Landscape of Hearing Loss in the Caribbean: A Narrative ReviewLéShon Peart, Mustafa Tekin
Frontiers in Bioscience (Landmark Edition)|June 2, 2012
Autosomal recessive nonsyndromic deafness genes: a reviewDuygu Duman, Mustafa Tekin
American Journal of Medical Genetics. Part A|April 21, 2007
Genetic epidemiological studies of congenital/prelingual deafness in Turkey: population structure and mating type are major determinants of mutation identificationMustafa Tekin, Zehra Serap Arici
Irish Journal of Medical Science|October 13, 2022
Breast cancer risk coordinators: Artificial intelligence-based density measurement and Mullerian-inhibiting substanceŞevki Pedük, Sevcan Sarıkaya, Mustafa Tekin
Journal of Human Genetics|November 8, 2013
The promise of whole-exome sequencing in medical geneticsBahareh Rabbani, Mustafa Tekin, Nejat Mahdieh
Balkan Medical Journal|May 28, 2019
Genetic Causes of Inner Ear Anomalies: a Review from the Turkish Study Group for Inner Ear AnomaliesEmre Ocak, Duygu Duman, Mustafa Tekin
American Journal of Medical Genetics. Part A|August 13, 2005
A novel missense mutation in a C2 domain of OTOF results in autosomal recessive auditory neuropathyMustafa Tekin, Duygu Akcayoz, Armagan Incesulu
Kulak Burun Bogaz Ihtisas Dergisi : KBB = Journal of Ear, Nose, and Throat|May 29, 2007
[Screening of the mitochondrial 12S rRNA (MTRNR1) gene in probands with sensorineural hearing loss]Yaprak E Cirçir, Armağan Incesulu, Mustafa Tekin
Annals of Saudi Medicine|December 15, 2015
Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndromeSeda Orenay-Boyacioglu, Mustafa Tekin, Munis Dundar
Orphanet Journal of Rare Diseases|December 21, 2017
KBG syndromeDayna Morel Swols, Joseph Foster, Mustafa Tekin
Pageof 24

Showing results (1-10 of 235) with videos related to

Sort By:
Pageof 24
Balkan Medical Journal|May 3, 2024
Genetic Landscape of Hearing Loss in the Caribbean: A Narrative ReviewLéShon Peart, Mustafa Tekin
Frontiers in Bioscience (Landmark Edition)|June 2, 2012
Autosomal recessive nonsyndromic deafness genes: a reviewDuygu Duman, Mustafa Tekin
American Journal of Medical Genetics. Part A|April 21, 2007
Genetic epidemiological studies of congenital/prelingual deafness in Turkey: population structure and mating type are major determinants of mutation identificationMustafa Tekin, Zehra Serap Arici
Irish Journal of Medical Science|October 13, 2022
Breast cancer risk coordinators: Artificial intelligence-based density measurement and Mullerian-inhibiting substanceŞevki Pedük, Sevcan Sarıkaya, Mustafa Tekin
Journal of Human Genetics|November 8, 2013
The promise of whole-exome sequencing in medical geneticsBahareh Rabbani, Mustafa Tekin, Nejat Mahdieh
Balkan Medical Journal|May 28, 2019
Genetic Causes of Inner Ear Anomalies: a Review from the Turkish Study Group for Inner Ear AnomaliesEmre Ocak, Duygu Duman, Mustafa Tekin
American Journal of Medical Genetics. Part A|August 13, 2005
A novel missense mutation in a C2 domain of OTOF results in autosomal recessive auditory neuropathyMustafa Tekin, Duygu Akcayoz, Armagan Incesulu
Kulak Burun Bogaz Ihtisas Dergisi : KBB = Journal of Ear, Nose, and Throat|May 29, 2007
[Screening of the mitochondrial 12S rRNA (MTRNR1) gene in probands with sensorineural hearing loss]Yaprak E Cirçir, Armağan Incesulu, Mustafa Tekin
Annals of Saudi Medicine|December 15, 2015
Autozygosity in a Turkish family with scoliosis, blindness, and arachnodactyly syndromeSeda Orenay-Boyacioglu, Mustafa Tekin, Munis Dundar
Orphanet Journal of Rare Diseases|December 21, 2017
KBG syndromeDayna Morel Swols, Joseph Foster, Mustafa Tekin
Pageof 24