subject area of
- Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events. Journal Articles
- Developmental changes in red cell creatine and free erythrocyte protoporphyrin in healthy premature infants during the first six months of life Journal Articles
- Diverse hematological phenotypes of β‐thalassemia carriers Journal Articles
- Evaluation of a Dual Hemoglobin A2/A1c Quantitation Kit on the Bio-Rad Variant II Automated Hemoglobin Analyzer Journal Articles
- Hb A2Hong Kong – A Novel δ-Globin Variant in a Chinese Family Masks the Diagnosis of β-Thalassemia Trait Journal Articles
- High Hb A2β-Thalassemia Due to a 468 bp Deletion in a Patient with Hb S/β-Thalassemia Journal Articles
- High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region. Journal Articles
- High hemoglobin A2 beta-thalassemia. Journal Articles
- Identification of a New δ Chain Hemoglobin Variant in a β-Thalassemia Carrier: Hb A2-MUMC [δ13(A10)Ala → Asp] Journal Articles
- Identification of hemoglobin E by the isopropanol solubility test Journal Articles
- Is HbA2 level a reliable diagnostic measurement for β‐thalassemia trait in people with iron deficiency? Journal Articles
- Laboratory diagnosis of HB CC-α-thalassemia Journal Articles
- Normal Hb A2β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) inCiswith the Hb A2’δ-Globin Gene Missense Mutation (HBD: c.49G>C) Journal Articles
- Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG orHBA1:c.2T>A) Journal Articles
- Sickle Cell Traits in Canada Journal Articles
- The genetics of hemoglobin A2 regulation in sickle cell anemia Journal Articles