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Hemoglobin|June 14, 2019
A Case of Hereditary Spherocytosis Caused by a Novel Homozygous Mutation in the SPTB Gene Misdiagnosed as β-Thalassemia Intermedia Due to a KLF1 Gene MutationKun Yang, Quan Ren, Yi Wu, et al.Hemoglobin|January 1, 1985
Prenatal diagnosis of thalassemia and of the hemoglobinopathies; a reviewD LoukopoulosHemoglobin|February 7, 2023
Prediction of Heart and Liver Iron Overload in β-Thalassemia Major Patients Using Machine Learning MethodsNaeimehossadat Asmarian, Alireza Kamalipour, Mahnaz Hosseini-Bensenjan, et al.Hemoglobin|November 11, 2022
Spectrum of β-Thalassemia and Other Hemoglobinopathies in the Saurashtra Region of Gujarat, India: Analysis of a Large Population Screening ProgramNishith A Vachhani, Daya J Vekariya, Roshan B Colah, et al.Hemoglobin|March 6, 2023
Celocentesis for Early Prenatal Diagnosis in Couples at-Risk for β-Thalassemia and Sicilian (δβ)0-ThalassemiaAntonino Giambona, Filippo Leto, Filippo Cassarà, et al.Hemoglobin|February 23, 2023
Genotype-Phenotype Study of β-Thalassemia Patients in SabahLatifah Suali, Falah Abass Mohammad Salih, Mohammad Yusof Ibrahim, et al.Hemoglobin|October 15, 2024
δβ-Thalassemia and α-Triplication: Is Genetic Retesting Worthwhile in Case of Non-Coherent Phenotype?Cristina Giubbilei, Simona D'Angelo, Ilaria Fotzi, et al.Hemoglobin|September 3, 2024
First Report of Hb Youngstown in Capillary Electrophoresis and Overlapping Hb Analysis Findings with Hb RushKim Yan Poh, Ping Chong BeePageof 240