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European Journal of Anaesthesiology
|
June 9, 2007
Prediction of difficult tracheal intubation in Turkish patients: a multi-center methodological study
T 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 dystocia
B Elmas, N Ercan, D T Ersak, et al.
Clinical Rheumatology
|
September 12, 2002
Antistreptococcal response is exaggerated in children with familial Mediterranean fever
F Yalçinkaya, E Ince, T Uçar, et al.
Clinical Genetics
|
November 8, 2017
Variants in CIB2 cause DFNB48 and not USH1J
K 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 deafness
X 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 Guatemala
C 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 microdontia
M 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 development
Anastassia Voronova, Denis Gallagher, Mark Zander, et al.
Neurology
|
September 26, 2007
Distal truncation of KCC3 in non-French Canadian HMSN/ACC families
A 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 study
Polat Dursun, Haluk Dervisoglu, Mine Daggez, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 92) with videos related to
Sort By:
Page
of 10
European Journal of Anaesthesiology
|
June 9, 2007
Prediction of difficult tracheal intubation in Turkish patients: a multi-center methodological study
T 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 dystocia
B Elmas, N Ercan, D T Ersak, et al.
Clinical Rheumatology
|
September 12, 2002
Antistreptococcal response is exaggerated in children with familial Mediterranean fever
F Yalçinkaya, E Ince, T Uçar, et al.
Clinical Genetics
|
November 8, 2017
Variants in CIB2 cause DFNB48 and not USH1J
K 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 deafness
X 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 Guatemala
C 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 microdontia
M 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 development
Anastassia Voronova, Denis Gallagher, Mark Zander, et al.
Neurology
|
September 26, 2007
Distal truncation of KCC3 in non-French Canadian HMSN/ACC families
A 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 study
Polat Dursun, Haluk Dervisoglu, Mine Daggez, et al.
Page
of 10