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C Altay

Showing results (111-120 of 160) with videos related to

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Haematologica|March 1, 1992
Beta-globin haplotype and XmnI polymorphism at position G (gamma)-158 and HbF production in Fanconi's anemiaM C Rosatelli, C Altay, R Oner, et al.
Hemoglobin|March 18, 2000
Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish familyF Gümrük, H Mergen, R Oner, et al.
Hemoglobin|January 17, 2002
Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: effects of haplotype on phenotypeE Birben, C Oner, R Oner, et al.
Pediatric Hematology and Oncology|March 1, 1996
Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experienceA Gürgey, S Beksaç, E Gümrük, et al.
Journal of Clinical Pathology|August 30, 2005
High cystine in platelets from patients with nephropathic cystinosis: a chemical, ultrastructural, and functional evaluationL Olcay, E Erdemli, M Kesimer, et al.
European Review for Medical and Pharmacological Sciences|June 17, 2024
Biochemical parameters and clinical outcomes of carbon monoxide poisoning in special groups: children, pregnant women, and the elderlyA Vural, T Dolanbay, M Ozçelik, et al.
American Journal of Hematology|July 30, 2004
Severe hemolytic anemia associated with Hb Volga [beta27(B9)Ala-->Asp]: GCC-->GAC at codon 27 in a Turkish familyM Sözen, C Karaaslan, R Oner, et al.
Cell|May 1, 1979
The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H diseaseS H Orkin, J Old, H Lazarus, et al.
Hemoglobin|May 1, 1995
Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrowA Gürgey, C Altay, L H Gu, et al.
Hemoglobin|January 1, 1988
Hb F-Baskent or alpha 2A gamma 128(H6)Ala----ThrC Altay, A Gurgey, J B Wilson, et al.
Pageof 16

Showing results (111-120 of 160) with videos related to

Sort By:
Pageof 16
Haematologica|March 1, 1992
Beta-globin haplotype and XmnI polymorphism at position G (gamma)-158 and HbF production in Fanconi's anemiaM C Rosatelli, C Altay, R Oner, et al.
Hemoglobin|March 18, 2000
Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish familyF Gümrük, H Mergen, R Oner, et al.
Hemoglobin|January 17, 2002
Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: effects of haplotype on phenotypeE Birben, C Oner, R Oner, et al.
Pediatric Hematology and Oncology|March 1, 1996
Prenatal diagnosis of hemoglobinopathies in Turkey: Hacettepe experienceA Gürgey, S Beksaç, E Gümrük, et al.
Journal of Clinical Pathology|August 30, 2005
High cystine in platelets from patients with nephropathic cystinosis: a chemical, ultrastructural, and functional evaluationL Olcay, E Erdemli, M Kesimer, et al.
European Review for Medical and Pharmacological Sciences|June 17, 2024
Biochemical parameters and clinical outcomes of carbon monoxide poisoning in special groups: children, pregnant women, and the elderlyA Vural, T Dolanbay, M Ozçelik, et al.
American Journal of Hematology|July 30, 2004
Severe hemolytic anemia associated with Hb Volga [beta27(B9)Ala-->Asp]: GCC-->GAC at codon 27 in a Turkish familyM Sözen, C Karaaslan, R Oner, et al.
Cell|May 1, 1979
The molecular basis of alpha-thalassemias: frequent occurrence of dysfunctional alpha loci among non-Asians with Hb H diseaseS H Orkin, J Old, H Lazarus, et al.
Hemoglobin|May 1, 1995
Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrowA Gürgey, C Altay, L H Gu, et al.
Hemoglobin|January 1, 1988
Hb F-Baskent or alpha 2A gamma 128(H6)Ala----ThrC Altay, A Gurgey, J B Wilson, et al.
Pageof 16