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M Tekin

Showing results (81-90 of 92) with videos related to

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European Journal of Anaesthesiology|June 9, 2007
Prediction of difficult tracheal intubation in Turkish patients: a multi-center methodological studyT S Yildiz, F Korkmaz, M Solak, et al.
Nigerian Journal of Clinical Practice|December 20, 2022
Risk factors for brachial plexus injury and permanent sequelae due to shoulder dystociaB Elmas, N Ercan, D T Ersak, et al.
Clinical Rheumatology|September 12, 2002
Antistreptococcal response is exaggerated in children with familial Mediterranean feverF Yalçinkaya, E Ince, T Uçar, et al.
Clinical Genetics|November 8, 2017
Variants in CIB2 cause DFNB48 and not USH1JK T Booth, K Kahrizi, M Babanejad, et al.
Human Molecular Genetics|December 14, 2001
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafnessX Z Liu, X J Xia, J Adams, et al.
Clinical Genetics|September 9, 2015
A Mayan founder mutation is a common cause of deafness in GuatemalaC Carranza, I Menendez, M Herrera, et al.
Clinical Genetics|April 26, 2008
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontiaM Tekin, H Oztürkmen Akay, S Fitoz, et al.
Springerplus|July 8, 2016
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentAnastassia Voronova, Denis Gallagher, Mark Zander, et al.
Neurology|September 26, 2007
Distal truncation of KCC3 in non-French Canadian HMSN/ACC familiesA Salin-Cantegrel, J-B Rivière, N Dupré, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|July 6, 2020
Performing gynecologic cancer surgery during the COVID-19 pandemic in Turkey: A multicenter retrospective observational studyPolat Dursun, Haluk Dervisoglu, Mine Daggez, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
European Journal of Anaesthesiology|June 9, 2007
Prediction of difficult tracheal intubation in Turkish patients: a multi-center methodological studyT S Yildiz, F Korkmaz, M Solak, et al.
Nigerian Journal of Clinical Practice|December 20, 2022
Risk factors for brachial plexus injury and permanent sequelae due to shoulder dystociaB Elmas, N Ercan, D T Ersak, et al.
Clinical Rheumatology|September 12, 2002
Antistreptococcal response is exaggerated in children with familial Mediterranean feverF Yalçinkaya, E Ince, T Uçar, et al.
Clinical Genetics|November 8, 2017
Variants in CIB2 cause DFNB48 and not USH1JK T Booth, K Kahrizi, M Babanejad, et al.
Human Molecular Genetics|December 14, 2001
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafnessX Z Liu, X J Xia, J Adams, et al.
Clinical Genetics|September 9, 2015
A Mayan founder mutation is a common cause of deafness in GuatemalaC Carranza, I Menendez, M Herrera, et al.
Clinical Genetics|April 26, 2008
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontiaM Tekin, H Oztürkmen Akay, S Fitoz, et al.
Springerplus|July 8, 2016
Ankrd11 is a chromatin regulator involved in autism that is essential for neural developmentAnastassia Voronova, Denis Gallagher, Mark Zander, et al.
Neurology|September 26, 2007
Distal truncation of KCC3 in non-French Canadian HMSN/ACC familiesA Salin-Cantegrel, J-B Rivière, N Dupré, et al.
International Journal of Gynaecology and Obstetrics: the Official Organ of the International Federation of Gynaecology and Obstetrics|July 6, 2020
Performing gynecologic cancer surgery during the COVID-19 pandemic in Turkey: A multicenter retrospective observational studyPolat Dursun, Haluk Dervisoglu, Mine Daggez, et al.
Pageof 10