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- Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease Academic Article
- Identification of hemoglobin E by the isopropanol solubility test Academic Article
- Laboratory diagnosis of HB CC-α-thalassemia Academic Article
- Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19G > A) and Hb Osu Christiansborg (HBB: c.157G > A) Academic Article