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Hemoglobin|June 28, 2019
A Novel Human β-Globin Gene Variant [Hb London-Ontario, HBB: c.332T>G] is Associated with Transfusion-Dependent Anemia in a Patient with a Hemoglobin Electrophoresis Pattern Consistent with β-Thalassemia TraitMarc N Bienz, Cyrus Hsia, John S Waye, et al.Hemoglobin|June 14, 2019
A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic AnemiaThomas R L Klei, Sima Kheradmand Kia, Martijn Veldthuis, et al.Hemoglobin|May 22, 2019
Polymorphisms of α-Globin Genes Compromise Polymerase Chain Reaction-Based α-Thalassemia Genotyping in Three Chinese FamiliesManna Sun, Jiwu Lou, Ying Zhag, et al.Hemoglobin|March 4, 2022
Profiling of 35 Cases of Hb S/Hb E (HBB: c.20A>T/HBB: c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, IndiaSnehadhini Dehury, Pradeep K Mohanty, Siris Patel, et al.Hemoglobin|October 11, 2019
Molecular Survey of Hemoglobinopathies in Myanmar Workers in Northeast Thailand Revealed an Unexpectedly High Prevalence of α+-ThalassemiaAye Chan Pyae, Hataichanok Srivorakun, Attawut Chaibunruang, et al.Hemoglobin|February 14, 2022
Glucose-6-Phosphate Dehydrogenase Deficiency: An Overview of the Prevalence and Genetic Variants in Saudi ArabiaHassan A HamaliHemoglobin|September 22, 2021
A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys, HBA2: c.55G>T]Ya-Li Lei, Yue-Mei Liang, Qun Cao, et al.Hemoglobin|March 19, 1999
The association of Hb Khartoum [beta124(H2)Pro-->Arg] with gamma+-thalassemia is responsible for hemolytic disease in the newborn of a Sudanese familyR A Bayoumi, A Dawodu, M M Qureshi, et al.Hemoglobin|January 1, 1986
Interaction of hemoglobin Siriraj with hemoglobin S: a mild sickle cell syndromeM D Rhoda, N Arous, M C Garel, et al.Hemoglobin|January 1, 1983
Hb S Mobile: a new genetic combinationR G Schneider, J Zusman, W B Smith, et al.Pageof 240