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European Journal of Pediatrics
|
February 25, 2010
A novel mutation of 5alpha-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment
Senay Savas Erdeve, Zehra Aycan, Merih Berberoglu, et al.
Plos One
|
November 30, 2016
Spatially Explicit Models to Investigate Geographic Patterns in the Distribution of Forensic STRs: Application to the North-Eastern Mediterranean
Francesco Messina, Andrea Finocchio, Nejat Akar, et al.
Pediatric Hematology and Oncology
|
July 16, 2005
Familial high factor VIII level in a child with necrotizing fasciitis complicating primary varicella infection
A Emin Kurekci, H Ibrahim Aydin, A Avni Atay, et al.
Journal of Cardiothoracic Surgery
|
September 30, 2011
Thrombotic gene polymorphisms and postoperative outcome after coronary artery bypass graft surgery
Ozan Emiroglu, Serkan Durdu, Yonca Egin, et al.
The Journal of Pediatrics
|
November 24, 2007
Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa
Fatoş Yalçinkaya, Z Birsin Ozçakar, Ozgür Kasapçopur, et al.
Scientific Reports
|
May 12, 2018
A finely resolved phylogeny of Y chromosome Hg J illuminates the processes of Phoenician and Greek colonizations in the Mediterranean
Andrea Finocchio, Beniamino Trombetta, Francesco Messina, et al.
Mikrobiyoloji Bulteni
|
August 12, 2022
[Investigation of Humoral and Cellular Immunity in TOBB ETÜ Hospital Workers After Three Doses of CoronaVac Vaccination and after One Dose of Comirnaty Vaccination Following Two Doses of CoronaVac]
Ferda Özyurda, Yasemin Ardıçoğlu Akışın, Tuğba Mert, et al.
Turkish Journal of Medical Sciences
|
September 7, 2020
Identification of novel TUBB1 variants in patients with macrothrombocytopenia
Zihni Onur Çalışkaner, Abdullah Abdul Waheed, Merve Tuzlakoğlu Öztürk, et al.
Journal of Pediatric Genetics
|
January 1, 2024
Genetic Profiling of Pediatric Patients with B-Cell Precursor Acute Lymphoblastic Leukemia
Dilara Fatma Akin-Bali, Beyza Doganay Erdogan, Deniz Aslar Oner, et al.
Medical Hypotheses
|
May 11, 2015
C-type lectin domain family 12, member A: A common denominator in Behçet's syndrome and acute gouty arthritis
Ali Kemal Oğuz, Seda Yılmaz, Nejat Akar, et al.
Page
of 23
Search research articles
Search
Showing results (201-210 of 229) with videos related to
Sort By:
Page
of 23
European Journal of Pediatrics
|
February 25, 2010
A novel mutation of 5alpha-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment
Senay Savas Erdeve, Zehra Aycan, Merih Berberoglu, et al.
Plos One
|
November 30, 2016
Spatially Explicit Models to Investigate Geographic Patterns in the Distribution of Forensic STRs: Application to the North-Eastern Mediterranean
Francesco Messina, Andrea Finocchio, Nejat Akar, et al.
Pediatric Hematology and Oncology
|
July 16, 2005
Familial high factor VIII level in a child with necrotizing fasciitis complicating primary varicella infection
A Emin Kurekci, H Ibrahim Aydin, A Avni Atay, et al.
Journal of Cardiothoracic Surgery
|
September 30, 2011
Thrombotic gene polymorphisms and postoperative outcome after coronary artery bypass graft surgery
Ozan Emiroglu, Serkan Durdu, Yonca Egin, et al.
The Journal of Pediatrics
|
November 24, 2007
Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa
Fatoş Yalçinkaya, Z Birsin Ozçakar, Ozgür Kasapçopur, et al.
Scientific Reports
|
May 12, 2018
A finely resolved phylogeny of Y chromosome Hg J illuminates the processes of Phoenician and Greek colonizations in the Mediterranean
Andrea Finocchio, Beniamino Trombetta, Francesco Messina, et al.
Mikrobiyoloji Bulteni
|
August 12, 2022
[Investigation of Humoral and Cellular Immunity in TOBB ETÜ Hospital Workers After Three Doses of CoronaVac Vaccination and after One Dose of Comirnaty Vaccination Following Two Doses of CoronaVac]
Ferda Özyurda, Yasemin Ardıçoğlu Akışın, Tuğba Mert, et al.
Turkish Journal of Medical Sciences
|
September 7, 2020
Identification of novel TUBB1 variants in patients with macrothrombocytopenia
Zihni Onur Çalışkaner, Abdullah Abdul Waheed, Merve Tuzlakoğlu Öztürk, et al.
Journal of Pediatric Genetics
|
January 1, 2024
Genetic Profiling of Pediatric Patients with B-Cell Precursor Acute Lymphoblastic Leukemia
Dilara Fatma Akin-Bali, Beyza Doganay Erdogan, Deniz Aslar Oner, et al.
Medical Hypotheses
|
May 11, 2015
C-type lectin domain family 12, member A: A common denominator in Behçet's syndrome and acute gouty arthritis
Ali Kemal Oğuz, Seda Yılmaz, Nejat Akar, et al.
Page
of 23