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Acta Haematologica|January 1, 1996
A novel (delta beta)(0)-thalassemia due to a approximately 30-kb deletion observed in a Turkish familyR Oner, C Oner, G Erdem, et al.Transfusion Medicine (Oxford, England)|May 21, 2015
Interleukin-6 and C-reactive protein load in pre-storage and post-storage white blood cell-filtered red blood cell transfusions in premature infantsB Say, F N Sari, S S Oguz, et al.Blood|January 1, 1989
An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin geneT A Stoming, G S Stoming, K D Lanclos, et al.The New England Journal of Medicine|July 27, 1978
Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemias caused by globin-gene deletionS H Orkin, B P Alter, C Altay, et al.Human Heredity|May 1, 1997
Genotype-phenotype analysis in HbS-beta-thalassemiaC Altay, C Oner, R Oner, et al.Human Genetics|May 1, 1989
The levels of zeta, gamma, and delta chains in patients with Hb H diseaseF Kutlar, J M Gonzalez-Redondo, A Kutlar, et al.Acta Endocrinologica (Bucharest, Romania : 2005)|May 8, 2023
NIVOLUMAB ASSOCIATED ENDOCRINE ABNORMALITIES: CHALLENGING CASES FROM A REFERENCE CLINICM C Unal, G Güngör Semiz, O Ozdoğan, et al.The Turkish Journal of Pediatrics|April 19, 2000
Autoimmune hemolytic anemia with warm antibodies in children: retrospective analysis of 51 casesA Gürgey, I Yenicesu, T Kanra, et al.Hemoglobin|January 1, 1991
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemiaR Oner, S Agarwal, A J Dimovski, et al.Journal of Chromatography|July 5, 1991
Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetusesF Kutlar, H Moscoso, C R Kiefer, et al.Pageof 16