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Hemoglobin|August 20, 2015
Acute Splenic Sequestration Crisis in Adult Sickle Cell Disease: A Report of 16 CasesLeonard Naymagon, Gopichand Pendurti, Henny H BillettHemoglobin|December 10, 2014
Characterization of Hb Lepore variants in the UK populationLina Guo, Anika Kausar, John M Old, et al.Hemoglobin|January 8, 2015
A new Aγ-globin chain variant: Hb F-Sykesville MD [Aγ113(G15)Val → Ile; HBG1: c.340G>A] detected in a Caucasian babyNiren Patel, Jason Fixler, Yoram Unguru, et al.Hemoglobin|January 10, 2015
The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patientSule Unal, David H K Chui, Hong-Yuan Luo, et al.Hemoglobin|January 10, 2015
Insulin resistance and β cell function in patients with β-thalassemia majorRobabeh Ghergherehchi, Afshin HabibzadehHemoglobin|January 10, 2015
Identification of a novel mutation in the β-globin gene 3' untranslated region (HBB: c.*+118A > G) in SpainMaria Ascensión Herrera, Félix De La Fuente-Gonzalo, Fernando Ataúlfo González, et al.Hemoglobin|July 25, 2015
The Effect of Nonsense Mediated Decay on Transcriptional Activity Within the Novel β-Thalassemia Mutation HBB: c.129delTLuke Forster, Rasha Mesbah Ardakani, Talal Qadah, et al.Hemoglobin|July 25, 2015
Incidence and Predictors of Bacterial infection in Febrile Children with Sickle Cell DiseaseBenita J Morrissey, Thomas P Bycroft, Ofran Almossawi, et al.Hemoglobin|August 27, 2014
The spectrum of β-thalassemia mutations in Hatay, Turkey: reporting three new mutationsOzgur Aldemir, Muzeyyen Izmirli, Hasan KayaHemoglobin|December 6, 2014
A new hemoglobin variant: Hb Meylan [β73(E17)Asp → Phe; HBB: c.220G>T; c.221A>T] with a double base mutation at the same codonCéline Renoux, Cécile Feray, Philippe Joly, et al.Pageof 238