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Prenatal Diagnosis of Thalassemia Intermedia: Is It Justified?
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 521, doi. 10.1111/j.1749-6632.1990.tb24351.x
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The Use of Direct Gene Analysis to Define β-Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 23, doi. 10.1111/j.1749-6632.1990.tb24287.x
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New Orally Effective Iron Chelators.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 351, doi. 10.1111/j.1749-6632.1990.tb24322.x
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Oral Iron Chelators for the Clinical Management of Iron Overload.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 311, doi. 10.1111/j.1749-6632.1990.tb24318.x
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β-Thalassemia Intermedia in Turkey.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 81, doi. 10.1111/j.1749-6632.1990.tb24293.x
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Retroviral Gene Transfer Using Safe and Efficient Packaging Cell Lines.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 407, doi. 10.1111/j.1749-6632.1990.tb24328.x
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Use of Central Venous Access for Iron Chelation Therapy<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 579, doi. 10.1111/j.1749-6632.1990.tb24372.x
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β-Thalassemia Mutations in Sicily<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 67, doi. 10.1111/j.1749-6632.1990.tb24291.x
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Pyridoxal Isonicotinoyl Hydrazone.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 315, doi. 10.1111/j.1749-6632.1990.tb24319.x
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A New Strategy for Direct Detection of β-Thalassemia Mutations.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 74, doi. 10.1111/j.1749-6632.1990.tb24292.x
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The Regulation of γ-Globin Gene Expression.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 160, doi. 10.1111/j.1749-6632.1990.tb24302.x
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Pharmacologic Manipulation of Fetal Hemoglobin in the Hemoglobinopathies<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 179, doi. 10.1111/j.1749-6632.1990.tb24304.x
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Fate of α-Hemoglobin Chains and Erythrocyte Defects in β-Thalassemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 106, doi. 10.1111/j.1749-6632.1990.tb24296.x
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Regulation of γ-Globin Expression in Hereditary Persistence of Fetal Hemoglobin.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 191, doi. 10.1111/j.1749-6632.1990.tb24306.x
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Design, Properties, and Effective Use of the Oral Chelator L1 and Other.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 339, doi. 10.1111/j.1749-6632.1990.tb24321.x
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Function of Transfected Globin Promoters and the Globin Locus Activator in K562 Erythroleukemia Cells<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 207, doi. 10.1111/j.1749-6632.1990.tb24308.x
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Family Reactions and Relationships in Thalassemia.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 451, doi. 10.1111/j.1749-6632.1990.tb24332.x
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Preface.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. xiii, doi. 10.1111/j.1749-6632.1990.tb24284.x
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Serum Erythropoietin Levels in β-Thalassemia.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 534, doi. 10.1111/j.1749-6632.1990.tb24357.x
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Cardiac Disease-free Survival in Patients with Thalassemia Major Treated with Subcutaneous Deferoxamine.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 585, doi. 10.1111/j.1749-6632.1990.tb24374.x
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A Psychosocial Perspective.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 442, doi. 10.1111/j.1749-6632.1990.tb24331.x
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The New Synthetic Hepatitis B Vaccine Administered at Low Doses by the Intradermal Route in Subjects at High Risk of Hepatitis B.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 556, doi. 10.1111/j.1749-6632.1990.tb24365.x
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Importance of House Calls in Detecting Heterozygotes in Families with Thalassemia.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 527, doi. 10.1111/j.1749-6632.1990.tb24354.x
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Screening for β-Thalassemia in Asian Indians by the Amplification-Refractory Mutation System.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 493, doi. 10.1111/j.1749-6632.1990.tb24341.x
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Immunodeficiency of β-Thalassemic Mice<sup>a,</sup><sup>b</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 538, doi. 10.1111/j.1749-6632.1990.tb24359.x
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HBED: A Potential Oral Iron Chelator<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 361, doi. 10.1111/j.1749-6632.1990.tb24323.x
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Protein S, Protein C, and Antithrombin III in Thrombotic Disease.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 549, doi. 10.1111/j.1749-6632.1990.tb24363.x
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A New Approach to Bone Marrow Transplantation in Thalassemia.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 394, doi. 10.1111/j.1749-6632.1990.tb24326.x
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Antenatal Diagnosis How to Deliver a Comprehensive Service in the United Kingdom.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 251, doi. 10.1111/j.1749-6632.1990.tb24312.x
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The α-Thalassemias.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 15, doi. 10.1111/j.1749-6632.1990.tb24286.x
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Metabolism of Non-Translatable Globin mRNAs Arising from Premature Translation Termination Codons.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 55, doi. 10.1111/j.1749-6632.1990.tb24290.x
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Gene Transfer into Murine Hematopoietic Stem Cells and Bone Marrow Stromal Cells.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 398, doi. 10.1111/j.1749-6632.1990.tb24327.x
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Antenatal Diagnosis of β-Thalassemia in Sardinia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 215, doi. 10.1111/j.1749-6632.1990.tb24309.x
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Localization and Characterization of the DNase I-Hypersensitive Site II (HS II) Enhancer.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 141, doi. 10.1111/j.1749-6632.1990.tb24300.x
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Evaluation of the Oral Iron Chelator 1,2-Dimethyl-3-hydroxypyrid-4-one (L1) in Iron-Loaded Patients<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 369, doi. 10.1111/j.1749-6632.1990.tb24324.x
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Prenatal Diagnosis of Thalassemia and of the Sickle Cell Syndromes in Greece<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 226, doi. 10.1111/j.1749-6632.1990.tb24310.x
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The Dominant Control Region of the Human β-Globin Domain.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 152, doi. 10.1111/j.1749-6632.1990.tb24301.x
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Antenatal Diagnosis Summary of Results<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 237, doi. 10.1111/j.1749-6632.1990.tb24311.x
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Stopping the Biologic Clock for Globin Gene Switching<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 134, doi. 10.1111/j.1749-6632.1990.tb24299.x
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A Model for Reactivation of Hemoglobin F Synthesis in Normal Adult Erythropoiesis<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 196, doi. 10.1111/j.1749-6632.1990.tb24307.x
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Analysis of Human γ-To-β Switching in Transgenic Mice<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 127, doi. 10.1111/j.1749-6632.1990.tb24298.x
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Expression of Human Globin Genes in Transgenic Mice Carrying the β-Globin Gene Cluster with a Mutation Causing <sup>G</sup>γβ<sup>+</sup> Hereditary Persistence of Fetal Hemoglobin<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 167, doi. 10.1111/j.1749-6632.1990.tb24303.x
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Somatomedin C and Zinc Status in β-Thalassemia Major.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 540, doi. 10.1111/j.1749-6632.1990.tb24360.x
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In Vivo Measurement of Hepatic and Cardiac Iron in Cooley's Anemia by Nuclear Resonance Scattering.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 573, doi. 10.1111/j.1749-6632.1990.tb24370.x
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Increase with Age in the Prevalence of β-Thalassemia Trait among Sicilians<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 504, doi. 10.1111/j.1749-6632.1990.tb24345.x
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A New System for Subcutaneous Infusion of Desferrioxamine.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 577, doi. 10.1111/j.1749-6632.1990.tb24371.x
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Sickle Cell Thalassemia in Greece.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 508, doi. 10.1111/j.1749-6632.1990.tb24346.x
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DNA Diagnosis of Thalassemias in Chinese by a Non-Radioactive Method<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 519, doi. 10.1111/j.1749-6632.1990.tb24350.x
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Changes in Spin-Lattice (T1) and Spin-Spin (T2) Relaxation Times of Packed Red Blood Cell Samples during Sixty Days at Room Temperature.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 559, doi. 10.1111/j.1749-6632.1990.tb24366.x
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Sardinian Haplotype II β<sup>0</sup>-Thalassemia Is Linked to the Variant <sup>A</sup>γ<sup>T</sup>-Globin Gene with a 4-Bp Promoter Deletion and Diminished <sup>A</sup>γ<sup>T</sup> Expression<sup>a,</sup><sup>b,</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 485, doi. 10.1111/j.1749-6632.1990.tb24338.x
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