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Hemoglobin|June 3, 2016
Hb Tianshui (HBB: C.119A > G) in Compound Heterozygosity with Hb S (HBB: C.20A > T) from Odisha, IndiaSatyabrata Meher, Snehadhini Dehury, Pradeep Kumar Mohanty, et al.Hemoglobin|November 11, 2017
Pre Gestational Thalassemia Screening in Mainland China: The First Two Years of a Preventive ProgramFan Jiang, Gui-Lan Chen, Jian Li, et al.Hemoglobin|November 29, 2017
Characterization of Two Novel Deletions Involving the 5' Region of the β-Globin GeneJohn S Waye, Meredith Hanna, Betty-Ann Hohenadel, et al.Hemoglobin|December 19, 2017
Coinheritance of α- and β-Thalassemia with a Novel Mutation (HBB: c.268_281delAGTGAGCTGCACTG) in a Chinese FamilyChuyun Cheng, Qi Peng, Siping Li, et al.Hemoglobin|December 19, 2017
Enhancing Effect of Hydroxyurea on Hb F in Sickle Cell Disease: Ten-Year Egyptian ExperienceIlham Youssry, Amina Abdel-Salam, Rania Ismail, et al.Hemoglobin|December 19, 2017
Hb A2-Tianhe (HBD: c.323G>A): First Report in a Chinese Family with Normal Hb A2-β-Thalassemia TraitGui-Lan Chen, Lv-Yin Huang, Jian-Ying Zhou, et al.Hemoglobin|January 1, 1988
Homozygous beta zero-39 mutation with thalassemia intermedia in northern Sardinia: clinical, hematological and molecular analysisL Oggiano, F Dore, P Pistidda, et al.Hemoglobin|September 4, 2020
Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous β-Thalassemia 3.5 kb DeletionsWanicha Tepakhan, Sataron Kanjanaopas, Korntip SrewaradachpisalHemoglobin|September 7, 2020
Molecular Genetic Analysis of α-Thalassemia in Hamadan Province, West IranKeivan Moradi, Mozaffar Aznab, Mostafa Biglari, et al.Hemoglobin|September 7, 2020
How I Treat Acute Chest Syndrome in Asthmatic Children with Sickle Cell Disease. A Practical ReviewPascal Almon, Narcisse ElengaPageof 240