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Hemoglobin|September 16, 2014
Characterization of Hb Calvino (HBB: c.406G > A): a new silent β-globin gene variant found in coexistence with α-thalassemia in a family of African originMaria Marsella, Gianluca Salvagno, Bernadetta Dolcini, et al.Hemoglobin|January 10, 2015
Cardiomyopathy associated with iron overload: how does iron enter myocytes and what are the implications for pharmacological therapy?Karn Wijarnpreecha, Sirinart Kumfu, Siriporn C Chattipakorn, et al.Hemoglobin|January 1, 1986
Beta-thalassemia: analysis of mRNA precursors of a mutant human globin gene with defective splicing using peripheral blood nucleated red blood cellsA Oppenheim, A Karsai, R Treisman, et al.Hemoglobin|October 19, 2017
First Report of Hb Kent [β37(C3)Trp→Cys (TGG>TGC) HBB: c.114G>C] in a Chinese FamilyNelson C N Chan, King-Ho Chow, Rico F Y Leung, et al.Hemoglobin|January 1, 1988
Prenatal diagnosis of thalassemia: experiences at the Shanghai Children's HospitalY T Zeng, S Z Huang, M L ZhangHemoglobin|August 26, 2017
α+-Thalassemia Caused by an 811 bp Deletion in Individuals from Nanning, Guangxi: A Report of Two CasesQiang Zhang, Mingli Xu, Wanjun Zhou, et al.Hemoglobin|September 6, 2017
A Plea for the Newborn Diagnosis of Hb S-Hereditary Persistence of Fetal HemoglobinGraham R Serjeant, Beryl E Serjeant, Ian R Hambleton, et al.Hemoglobin|September 25, 2015
Mutation Spectrum of β-Thalassemia and Other Hemoglobinopathies in Chittagong, Southeast BangladeshTridip Chatterjee, Amit Chakravarty, Sudipa Chakravarty, et al.Hemoglobin|July 27, 2017
Prevalence of Thalassemia Traits and Iron Deficiency Anemia in Sindh, PakistanAbdul H Kandhro, Virapong Prachayasittikul, Chartchalerm Isarankura Na-Ayudhya, et al.Hemoglobin|August 10, 2017
Coinheritance of High Oxygen Affinity Hb Helsinki [HBB: c.248A>T; β82(EF6)Lys→Met] with Hb H DiseaseShir-Ying Lee, Jia-Hui Goh, Karen M L Tan, et al.Pageof 239