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Hemoglobin|March 8, 2019
First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian FamilyHossam Murad, Faten MoassasHemoglobin|November 14, 2018
Prevalence of α-Thalassemia in the Egyptian PopulationIlham Youssry, Ayman El Badawy, Rania M Samy, et al.Hemoglobin|August 23, 2019
Hb Guangxi [β65(E9)Lys→Glu (AAG>GAG); HBB: c.196A>G]: A Novel β-Globin VariantMiao Xu, Wei-Dong Chen, Ya-Jun Wang, et al.Hemoglobin|January 22, 2021
Comparison of Hematopoietic Stem Cell Transplantation Results in Patients with β-Thalassemia Major from Three Different Graft TypesSelime Aydogdu, Ersin Toret, Basak A Aksoy, et al.Hemoglobin|April 18, 2017
The Hb E (HBB: c.79G>A), Mean Corpuscular Volume, Mean Corpuscular Hemoglobin Cutoff Points in Double Heterozygous Hb E/- -SEA α-Thalassemia-1 Carriers are Dependent on Hemoglobin LevelsPrapapun Leckngam, Ektong Limweeraprajak, Tiemjan Kiewkarnkha, et al.Hemoglobin|September 14, 2011
Novel therapies targeting the endothelium in sickle cell diseaseCarolyn C HoppeHemoglobin|February 3, 2012
Is the poly A (T>C) mutation a causative factor for misdiagnosis in second trimester prenatal diagnosis of β-thalassemia by fetal blood analysis on high performance liquid chromatography?Khushnooma Y Italia, Pratibha M Sawant, Anita H Nadkarni, et al.Hemoglobin|January 12, 2012
A novel 26 bp deletion [HBB: c.20_45del26bp] in exon 1 of the β-globin gene causing β-thalassemia majorEunice S Edison, Rajkumar S Venkatesan, Sankari Devi Govindanattar, et al.Hemoglobin|December 8, 2011
Hb H disease with various β hemoglobinopathies: molecular, hematological and diagnostic aspectsSupan Fucharoen, Goonnapa FucharoenPageof 240