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Hemoglobin|September 4, 2018
Description of a Rare β-Globin Gene Mutation: -86 (C>G) (HBB: c.-136C>G) Observed in a Syrian FamilyFaten Moassas, Ayman Alabloog, Hossam MuradHemoglobin|September 8, 2018
Development of Visual Detection of α-Thalassemia-1 (the - -SEA Deletion) Using pH-Sensitive Loop-Mediated Isothermal AmplificationSirinart Chomean, Kanokporn Pholyiam, Areenuch Thamwarokun, et al.Hemoglobin|September 13, 2018
KFL1 Gene Variants in α-Thalassemia Individuals with Increased Fetal Hemoglobin in a Chinese PopulationFan Jiang, Yan-Xia Qu, Gui-Lan Chen, et al.Hemoglobin|March 24, 2022
A Novel Hemoglobin Variant Hb Liaobu [α107(G14)Val→Leu, HBA2: c.322G>C] Detected by Matrix-Assisted Laser Desorption Ionization-Time-of-Flight Mass SpectrometryXue-Mei Tan, Yan-Hui Liu, Xuan Shang, et al.Hemoglobin|September 12, 2018
Molecular Characterization of β-Thalassemia Mutations Via the Amplification Refractory Mutation System-Polymerase Chain Reaction Method at the North Waziristan Agency, PakistanNoor M Khan, Shoaib Ur Rehman, Muhammad Shakeel, et al.Hemoglobin|September 12, 2018
Compound Heterozygosity of β-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, IndiaAditya N Jha, Hrishikesh Mishra, Henu K Verma, et al.Hemoglobin|July 27, 2018
Characterization of Two Deep Intronic Variants on the β-Globin Gene with Inconsistent Interpretations of Clinical SignificanceRuna M Grimholt, Cornelis L Harteveld, Sandra G J Arkesteijn, et al.Hemoglobin|March 18, 2000
Identification of three rare beta-thalassemia mutations in the Pakistani populationS N Khan, S Riazuddin, R GalanelloHemoglobin|March 18, 2000
Hb Sallanches [alpha104(G11)Cys-->Tyr]: a rare alpha2-globin chain variant found in the homozygous state in three members of a Pakistani familyS N Khan, F I Butt, S Riazuddin, et al.Hemoglobin|May 21, 1999
The beta+-thalassemia mutation [IVS-II-5 (G-->C] creates an alternative splicing site in the second intervening sequenceN H Jiang, S LiangPageof 240