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Hemoglobin|January 14, 2012
Prenatal diagnosis of hemoglobinopathies by pyrosequencing: a more sensitive and rapid approach to fetal genotypingAdele T Timbs, Michelle J Rugless, Alice E Gallienne, et al.Hemoglobin|January 14, 2012
Screening for common nondeletional α-thalassemias in Chinese newborns by determination of Hb Bart's using the Sebia Capillarys 2 electrophoresis systemHai-Shen Tang, Jian-Ying Zhou, Xing-Mei Xie, et al.Hemoglobin|March 29, 2012
Microsatellite markers within the α-globin gene cluster for robust preimplantation genetic diagnosis of severe α-thalassemia syndromes in Mediterranean populationsAspasia Destouni, George Christopoulos, Christina Vrettou, et al.Hemoglobin|March 22, 2012
A novel case of Hb Phnom Penh: codons 117/118 (+ATC) as a cause of α+ -thalassemiaYin-Sheng Zhai, Hai-Shen Tang, Jian-Ying Zhou, et al.Hemoglobin|November 30, 2011
Novel α2 gene deletion (c.349_359 del GAGTTCACCCC) identified in association with the -α3.7 deletionStephen O Brennan, Tim Chan, Jaine DuncanHemoglobin|April 10, 2012
Coenzyme Q10 levels in β-thalassemia and its association with ferritin levels and chelation therapyCigdem Karakukcu, Musa Karakukcu, Ekrem Unal, et al.Hemoglobin|March 2, 2012
α(+)-Thalassemia trait caused by a frameshift mutation in exon 2 of the α2-globin gene [HBA2 c.244delT]John S Waye, Lynda Walker, Barry EngHemoglobin|November 19, 2014
Erythropoietin levels in patients with sickle cell disease do not correlate with known inducers of erythropoietinE Dianne Pulte, Steven E McKenzie, Jaime Caro, et al.Hemoglobin|November 19, 2014
Mutational spectrum of thalassemias and other hemoglobinopathies in West Bengal, Eastern IndiaTridip Chatterjee, Amit Chakravarty, Sudipa ChakravartyHemoglobin|September 7, 2000
Hb Bart's levels in cord blood and alpha-thalassemia mutations in CyprusK Kyriacou, A Kyrri, E Kalogirou, et al.Pageof 240