16 results on '"Felice, A. E."'
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2. Hb Valletta [β87(F3)Thr→Pro] and Hb Marseille/Long Island [β2(NA2)His→Pro; (–1)Met-(+1)Val-(+2)Pro-Leu], in a Unique Compound Heterozygote with a Normal Hemoglobin Phenotype
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3. An Electronic Infrastructure for Research and Treatment of the Thalassemias and Other Hemoglobinopathies: The Euro-Mediterranean Ithanet Project
4. A Review ofCis-TransInterplay Between DNA Sequences 5′ to theGγ- and β-Globin Genes Among Hb F-Malta-I Heterozygotes/Homozygotes and β-Thalassemia Homozygotes/Compound Heterozygotes, and the Effects of Hydroxyurea on the Hb F/F-Erythrocyte; the Need for Large Multicenter Trials
5. Developmental Effect of theXmnI Site onGγ-Globin Gene Expression Among Newborn Hb F-Malta-I [Gγ117(G19)His→Arg, CAT→CGT] Heterozygotes and Adult β+-Thalassemia Homozygotes
6. Characterization and locus assignment of two α-globin variants present in the maltese population: Hb St. Luke's [α95(G2)Pro→Arg] and Hb Setif [α94(G1)Asp→Tyr]
7. ComparativeIn VivoExpression of β+-Thalassemia Alleles
8. HB Setif [α94(GI)ASPàTYR] in Malta
9. Alternate Organization of α G-Philadelphia Globin Genes Among U.S. Black and Italian Caucasian Heterozygotes
10. Adult and Fetal Hemoglobin Production in Erythroid Colonies from Subjects with β-Thalassemia or with Hereditary Persistence of Fetal Hemoglobin (HPFH)
11. Observations on the Calculated Contents of Variant and Normal α Chains in Adult and Fetal Erythrocytes
12. Clinical and Hematological Evaluation of two δ0δ0- Thalassemia Homozygotes
13. Hb Evans or α262(E11)Val→Metβ2; an Unstable Hemoglobin Causing a Mild Hemolytic Anemia
14. The W.A. Schroeder Symposium on the Application of Hplc in Hemoglobin Analysis
15. Letter to the Editor
16. δβ-Thalassemia in a Mexican Family: Clinical Differences Among Homozygotes
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