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Genetic Counseling (Geneva, Switzerland)
|
January 24, 2004
Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) gene
M Tekin, T Duman, G Boğoçlu, et al.
QJM : Monthly Journal of the Association of Physicians
|
October 13, 2000
Familial Mediterranean fever and systemic amyloidosis in untreated Turkish patients
F Yalçinkaya, M Tekin, N Cakar, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
September 10, 1998
Coexistence of chronic discoid lupus erythematosus and sensorineural deafness
M Harman, H S Inalöz, M Tekin, et al.
Immunotherapy Advances
|
May 19, 2025
Therapeutic targeting of tumour-associated macrophage receptors
Rosa Gomes Alves Martins, Mehmet M Tekin, Mark S Cragg, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
March 10, 2000
Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis
M Tekin, F Yalçinkaya, N Tümer, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 11, 2000
Counseling dilemmas in EEC syndrome
M Tekin, C Ohle, D E Johnson, et al.
The Journal of Laryngology and Otology
|
January 25, 2019
Evaluation of the academic productivity of the top 100 worldwide physicians in the field of otorhinolaryngology and head and neck surgery using the Google Scholar h-index as the bibliometrics ranking system
M T Kalcioglu, Y Ileri, O I Ozdamar, et al.
Acta Anaesthesiologica Scandinavica
|
May 12, 2009
A new supraglottic airway device: LMA-supreme, comparison with LMA-Proseal
T Hosten, Y Gurkan, D Ozdamar, et al.
Auris, Nasus, Larynx
|
March 25, 2000
Facial neuroma in the internal auditory canal
C Mutlu, D R Djeric, M Tekin, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 3, 2014
Branchio-oculo-facial syndrome in a newborn caused by a novel TFAP2A mutation
N Günes, F B Cengiz, D Duman, et al.
Page
of 10
Search research articles
Search
Showing results (31-40 of 92) with videos related to
Sort By:
Page
of 10
Genetic Counseling (Geneva, Switzerland)
|
January 24, 2004
Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) gene
M Tekin, T Duman, G Boğoçlu, et al.
QJM : Monthly Journal of the Association of Physicians
|
October 13, 2000
Familial Mediterranean fever and systemic amyloidosis in untreated Turkish patients
F Yalçinkaya, M Tekin, N Cakar, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
September 10, 1998
Coexistence of chronic discoid lupus erythematosus and sensorineural deafness
M Harman, H S Inalöz, M Tekin, et al.
Immunotherapy Advances
|
May 19, 2025
Therapeutic targeting of tumour-associated macrophage receptors
Rosa Gomes Alves Martins, Mehmet M Tekin, Mark S Cragg, et al.
Acta Paediatrica (Oslo, Norway : 1992)
|
March 10, 2000
Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis
M Tekin, F Yalçinkaya, N Tümer, et al.
Genetic Counseling (Geneva, Switzerland)
|
April 11, 2000
Counseling dilemmas in EEC syndrome
M Tekin, C Ohle, D E Johnson, et al.
The Journal of Laryngology and Otology
|
January 25, 2019
Evaluation of the academic productivity of the top 100 worldwide physicians in the field of otorhinolaryngology and head and neck surgery using the Google Scholar h-index as the bibliometrics ranking system
M T Kalcioglu, Y Ileri, O I Ozdamar, et al.
Acta Anaesthesiologica Scandinavica
|
May 12, 2009
A new supraglottic airway device: LMA-supreme, comparison with LMA-Proseal
T Hosten, Y Gurkan, D Ozdamar, et al.
Auris, Nasus, Larynx
|
March 25, 2000
Facial neuroma in the internal auditory canal
C Mutlu, D R Djeric, M Tekin, et al.
Genetic Counseling (Geneva, Switzerland)
|
May 3, 2014
Branchio-oculo-facial syndrome in a newborn caused by a novel TFAP2A mutation
N Günes, F B Cengiz, D Duman, et al.
Page
of 10