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Acta Haematologica
|
January 1, 1973
Hereditary persistence of fetal hemoglobin and beta-thalassemia in a Turkish child
B Yamak, S Ozsoylu, C Altay, et al.
British Journal of Haematology
|
May 3, 2000
Prevalence of the prothrombin gene G20210A mutation in Azerbaijan
J Togrul, R Rustamov, A Gurgey, et al.
The Turkish Journal of Pediatrics
|
January 1, 1990
Acute lymphoblastic leukemia in a child with hemoglobins S and Q-Iran
A Gürgey, S Ozsoylu, G Hiçsönmez, et al.
Diagnostic and Interventional Imaging
|
July 19, 2016
Imaging findings of paraurethral leiomyoma
C Altay, O Bozkurt, M Secil, et al.
Journal of Medicine
|
January 1, 1994
Chronic autoimmune hemolytic anemia in children: a report of four patients
F Duru, A Gürgey, M Cetin, et al.
Pediatric Hematology and Oncology
|
September 1, 1994
Convulsion after blood transfusion in four beta-thalassemia intermedia patients
A Gürgey, O Kalayci, F Gümrük, et al.
British Journal of Haematology
|
February 23, 1999
Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous family
A Koc, J C Pronk, M Alikasifoglu, et al.
Thrombosis and Haemostasis
|
August 26, 2000
The factor V Leiden and prothrombin G20210A mutations in Kirghiz population
A Gurgey, D K Kudayarov, M Tuncer, et al.
Pediatric Research
|
August 1, 1981
alpha-thalassemia-2 and the variability of hematological values in children with sickle cell anemia
C Altay, M E Gravely, B R Joseph, et al.
Thrombosis Research
|
March 15, 2001
Evidence for the existence of the PAF acetylhydrolase mutation (Val279Phe) in non-Japanese populations: a preliminary study in Turkey, Azerbaijan, and Kyrgyzstan
G Balta, A Gurgey, D K Kudayarov, et al.
Page
of 16
Search research articles
Search
Showing results (61-70 of 160) with videos related to
Sort By:
Page
of 16
Acta Haematologica
|
January 1, 1973
Hereditary persistence of fetal hemoglobin and beta-thalassemia in a Turkish child
B Yamak, S Ozsoylu, C Altay, et al.
British Journal of Haematology
|
May 3, 2000
Prevalence of the prothrombin gene G20210A mutation in Azerbaijan
J Togrul, R Rustamov, A Gurgey, et al.
The Turkish Journal of Pediatrics
|
January 1, 1990
Acute lymphoblastic leukemia in a child with hemoglobins S and Q-Iran
A Gürgey, S Ozsoylu, G Hiçsönmez, et al.
Diagnostic and Interventional Imaging
|
July 19, 2016
Imaging findings of paraurethral leiomyoma
C Altay, O Bozkurt, M Secil, et al.
Journal of Medicine
|
January 1, 1994
Chronic autoimmune hemolytic anemia in children: a report of four patients
F Duru, A Gürgey, M Cetin, et al.
Pediatric Hematology and Oncology
|
September 1, 1994
Convulsion after blood transfusion in four beta-thalassemia intermedia patients
A Gürgey, O Kalayci, F Gümrük, et al.
British Journal of Haematology
|
February 23, 1999
Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous family
A Koc, J C Pronk, M Alikasifoglu, et al.
Thrombosis and Haemostasis
|
August 26, 2000
The factor V Leiden and prothrombin G20210A mutations in Kirghiz population
A Gurgey, D K Kudayarov, M Tuncer, et al.
Pediatric Research
|
August 1, 1981
alpha-thalassemia-2 and the variability of hematological values in children with sickle cell anemia
C Altay, M E Gravely, B R Joseph, et al.
Thrombosis Research
|
March 15, 2001
Evidence for the existence of the PAF acetylhydrolase mutation (Val279Phe) in non-Japanese populations: a preliminary study in Turkey, Azerbaijan, and Kyrgyzstan
G Balta, A Gurgey, D K Kudayarov, et al.
Page
of 16