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Research in Veterinary Science
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April 2, 2023
Relationship between periparturient diseases, metabolic markers and the dynamics of hair cortisol concentrations in dairy cows
M Tekin, D R Câmara, T M Binz, et al.
Clinical Genetics
|
September 17, 2003
Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey
M Tekin, D Akçayöz, E Comak, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
August 30, 2000
Tympanic membrane and middle ear pathologic correlates in mucoid otitis media
M Tekin, C Mutlu, M M Paparella, et al.
Pediatric Cardiology
|
September 25, 2007
The effect of p.Arg25Cys alteration in NKX2-5 on conotruncal heart anomalies: mutation or polymorphism?
M I Akçaboy, F B Cengiz, B Inceoğlu, et al.
The British Journal of Dermatology
|
June 15, 2011
Cardiomyopathy with alopecia and palmoplantar keratoderma (CAPK) is caused by a JUP mutation
H Erken, K O Yariz, D Duman, et al.
Clinical Genetics
|
February 26, 2011
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss
K O Yariz, T Walsh, H Akay, et al.
Balkan Journal of Medical Genetics : BJMG
|
October 28, 2016
Prevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey
A Uludağ, A Uysal, A Uludağ, et al.
American Journal of Medical Genetics
|
November 15, 2000
Fluorescence in situ hybridization detectable mosaicism for Angelman syndrome with biparental methylation
M Tekin, C Jackson-Cook, A Buller, et al.
Frontiers in Pediatrics
|
July 5, 2023
Comprehensiveness of online sources for patient education on hereditary hearing impairment
Yaşar Kemal Duymaz, Ahmet M Tekin, Patrick D'Haese, et al.
Clinical Genetics
|
May 15, 2009
A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia
A Sirmaci, H Oztürkmen-Akay, S Erbek, et al.
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of 10
Search research articles
Search
Showing results (51-60 of 92) with videos related to
Sort By:
Page
of 10
Research in Veterinary Science
|
April 2, 2023
Relationship between periparturient diseases, metabolic markers and the dynamics of hair cortisol concentrations in dairy cows
M Tekin, D R Câmara, T M Binz, et al.
Clinical Genetics
|
September 17, 2003
Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey
M Tekin, D Akçayöz, E Comak, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery
|
August 30, 2000
Tympanic membrane and middle ear pathologic correlates in mucoid otitis media
M Tekin, C Mutlu, M M Paparella, et al.
Pediatric Cardiology
|
September 25, 2007
The effect of p.Arg25Cys alteration in NKX2-5 on conotruncal heart anomalies: mutation or polymorphism?
M I Akçaboy, F B Cengiz, B Inceoğlu, et al.
The British Journal of Dermatology
|
June 15, 2011
Cardiomyopathy with alopecia and palmoplantar keratoderma (CAPK) is caused by a JUP mutation
H Erken, K O Yariz, D Duman, et al.
Clinical Genetics
|
February 26, 2011
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss
K O Yariz, T Walsh, H Akay, et al.
Balkan Journal of Medical Genetics : BJMG
|
October 28, 2016
Prevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey
A Uludağ, A Uysal, A Uludağ, et al.
American Journal of Medical Genetics
|
November 15, 2000
Fluorescence in situ hybridization detectable mosaicism for Angelman syndrome with biparental methylation
M Tekin, C Jackson-Cook, A Buller, et al.
Frontiers in Pediatrics
|
July 5, 2023
Comprehensiveness of online sources for patient education on hereditary hearing impairment
Yaşar Kemal Duymaz, Ahmet M Tekin, Patrick D'Haese, et al.
Clinical Genetics
|
May 15, 2009
A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia
A Sirmaci, H Oztürkmen-Akay, S Erbek, et al.
Page
of 10