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Hemoglobin|January 24, 2019
Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian PatientsHossam Murad, Faten Moassas, Ifad Ghoury, et al.Hemoglobin|January 16, 2020
A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB: c.92+6T>G] in a Chinese FamilyHaiyan Luo, Yongyi Zou, Yanqiu LiuHemoglobin|February 1, 2020
Nondeletional α-Thalassemia: Two New Mutations on the α2 GenePaloma Ropero, Jaime Arbeteta, Jorge M Nieto, et al.Hemoglobin|December 4, 2018
Efficacy of the National Thalassaemia and Sickle Cell Disease Prevention Programme in Northern Greece: 15-Year Experience, Practice and Policy Gaps for Natives and MigrantsStamatia Theodoridou, Nikolaos Prapas, Angeliki Balassopoulou, et al.Hemoglobin|December 19, 2018
The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the LiteratureKaren G Scheps, Viviana Varela, Héctor M TargovnikHemoglobin|January 5, 2020
Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central IranZahra Sajadpour, Zeinab Amini-Farsani, Majid Motovali-Bashi, et al.Hemoglobin|January 25, 2020
An Unusual Compound Heterozygosity for Hb O-Arab (HBB: c.364G>A) and Hb D-Los Angeles (HBB: c.364G>C)Adriaan J van Gammeren, Leonie Pelkmans, Corné C W van Endschot, et al.Hemoglobin|October 29, 2019
A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AGT>AGG); HBB: c.270T>G] Resulting in Hemoglobin VanderbiltWilliam Shomali, Rondeep Brar, Subramanyeswara R Arekapudi, et al.Hemoglobin|June 1, 2005
Molecular and clinical features of Hb H disease in northern ThailandPimlak Charoenkwan, Rawee Taweephon, Rattika Sae-Tung, et al.Pageof 240