Showing results (1571-1580 of 2,379) with videos related to
Sort By:
Pageof 238
Hemoglobin|December 6, 2014
Hb Souli, a 6 bp in-frame deletion on the HBA2 gene (HBA2: c.[41-46delCCTGGG]) leads to α-thalassemia intermedia, when in trans to a single α-globin gene deletionAntonis Kattamis, Polyxeni Delaporta, Irene Fylaktou, et al.Hemoglobin|December 20, 2014
β-globin genes: mutation hot-spots in the global thalassemia beltRakesh Kumar, Chandan Sagar, Dharmesh Sharma, et al.Hemoglobin|November 19, 2014
Prevalence of β-thalassemia trait and abnormal hemoglobins in Sanliurfa Province in southeast TurkeyAdnan Incebiyik, Ahmet Genc, Nese Gul Hilali, et al.Hemoglobin|November 19, 2014
Non-thalassemic phenotype associated with the -83 (G > A) mutation of the β-globin gene promoter (HBB: c.-133G > A)John S Waye, Barry Eng, Meredith Hanna, et al.Hemoglobin|January 15, 2020
Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene <i>HBA2</i>: c.1A>G MutationXingyuan Chen, Shiqiang Luo, Jun Huang, et al.Hemoglobin|November 9, 2020
Transcranial Doppler Velocities among Sickle Cell Disease Patients in Steady StateKhaled Salama, Rasha Rady, Rania H Hashem, et al.Hemoglobin|September 3, 2020
Receptor Activator of Nuclear Factor κ-Β Ligand/Osteoprotegerin Axis in Adults with Hb S/β-Thalassemia and β-Thalassemia TraitAnil Tombak, Burcu Boztepe, Serin Akbayir, et al.Hemoglobin|January 1, 1988
Newer developments in the identification of beta-thalassemiaT A Stoming, J C Diaz-Chico, K G Yang, et al.Hemoglobin|January 1, 1988
Treatment of the thalassemia syndrome with splenectomyX Y Yang, Q Qu, T Y Yang, et al.Hemoglobin|January 1, 1988
Beta-thalassemia in China: a systematic molecular characterization of beta-thalassemia mutationsS Huang, P G Waber, C E Dowling, et al.Pageof 238