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C Altay

Showing results (61-70 of 160) with videos related to

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Acta Haematologica|January 1, 1973
Hereditary persistence of fetal hemoglobin and beta-thalassemia in a Turkish childB Yamak, S Ozsoylu, C Altay, et al.
British Journal of Haematology|May 3, 2000
Prevalence of the prothrombin gene G20210A mutation in AzerbaijanJ 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-IranA Gürgey, S Ozsoylu, G Hiçsönmez, et al.
Diagnostic and Interventional Imaging|July 19, 2016
Imaging findings of paraurethral leiomyomaC Altay, O Bozkurt, M Secil, et al.
Journal of Medicine|January 1, 1994
Chronic autoimmune hemolytic anemia in children: a report of four patientsF Duru, A Gürgey, M Cetin, et al.
Pediatric Hematology and Oncology|September 1, 1994
Convulsion after blood transfusion in four beta-thalassemia intermedia patientsA 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 familyA Koc, J C Pronk, M Alikasifoglu, et al.
Thrombosis and Haemostasis|August 26, 2000
The factor V Leiden and prothrombin G20210A mutations in Kirghiz populationA 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 anemiaC 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 KyrgyzstanG Balta, A Gurgey, D K Kudayarov, et al.
Pageof 16

Showing results (61-70 of 160) with videos related to

Sort By:
Pageof 16
Acta Haematologica|January 1, 1973
Hereditary persistence of fetal hemoglobin and beta-thalassemia in a Turkish childB Yamak, S Ozsoylu, C Altay, et al.
British Journal of Haematology|May 3, 2000
Prevalence of the prothrombin gene G20210A mutation in AzerbaijanJ 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-IranA Gürgey, S Ozsoylu, G Hiçsönmez, et al.
Diagnostic and Interventional Imaging|July 19, 2016
Imaging findings of paraurethral leiomyomaC Altay, O Bozkurt, M Secil, et al.
Journal of Medicine|January 1, 1994
Chronic autoimmune hemolytic anemia in children: a report of four patientsF Duru, A Gürgey, M Cetin, et al.
Pediatric Hematology and Oncology|September 1, 1994
Convulsion after blood transfusion in four beta-thalassemia intermedia patientsA 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 familyA Koc, J C Pronk, M Alikasifoglu, et al.
Thrombosis and Haemostasis|August 26, 2000
The factor V Leiden and prothrombin G20210A mutations in Kirghiz populationA 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 anemiaC 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 KyrgyzstanG Balta, A Gurgey, D K Kudayarov, et al.
Pageof 16