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Hemoglobin|January 1, 1986
HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black familyJ E Bowman, R Bloom, S S Chen, et al.Hemoglobin|January 1, 1985
The separation of globin chains by high pressure cation exchange chromatographyS O BrennanHemoglobin|June 10, 2025
A Novel Large Deletion Including the Major Regulatory Element Compounded with SEA Deletion Causing Hydrops-Fetalis-SyndromePing Liu, Jieyu Wang, Hongyu Luo, et al.Hemoglobin|June 8, 2025
Hb A2-Getafe [δ 132 (H10) Lys > Thr, HBD: c.88C > A]: New Mutation in the δ-Globin Gene in a Spanish PatientRamiro Antonio Torrado Carrión, Rafael López Moreno, Carmen Blanco Barros, et al.Hemoglobin|July 20, 2025
Novel Double Heterozygosity: HBA2: c.70G > A (Hb Chad)/HBB: c.-78A > G and Novel Compound Heterozygosity: HBA2: c.70G > A (Hb Chad)/HBA1: c.84G > T (Hb Hekinan II) Hemoglobinopathy in a Chinese FamilyChao Ye, Jilin Qing, Yan Wei, et al.Hemoglobin|June 1, 2025
Unraveling Hemoglobin D's Influence: A Comprehensive Analysis of Clinicopathological Parameters in Hemoglobin D PatientsMohib Shamoon, Rafia Mahmood, Manzar Bozdar, et al.Hemoglobin|June 4, 2025
A Hemoglobin Variant, Resulting from a Novel Missense Mutation [CD 112(G14) Cys > Ser (TGT > TCT); HBB: C.338G > C], Was Discovered by MALDI-TOF MSWeijie Xie, Cheng Lin, Yueying Huang, et al.Hemoglobin|October 20, 2025
Utility of Molecular Sequencing and Hematologic Parameters for Diagnosis of α-Thalassemia: A Perspective of the National Reference LaboratoryRyan Shean, Nicole Deshmukh, Michael Palmer, et al.Hemoglobin|October 5, 2025
Hemoglobin Dieppe (HBB:c. 383A > G): A Rare Dominant β-Thalassemia in an Iraqi Kurdish FamilyTara Jamel Osman, Ashna H Karim, Rozhgar A Khailany, et al.Hemoglobin|July 7, 2025
HBA2: C.4delG: A Novel Frameshift Mutation Causing α+-Thalassemia Found in a Chinese FamilyWei Li, Guixi Wei, Shan Ren, et al.Pageof 240