subject area of
- A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells Journal Articles
- A Novel Human β-Globin Gene Variant [Hb London-Ontario,HBB: c.332T>G] is Associated with Transfusion-Dependent Anemia in a Patient with a Hemoglobin Electrophoresis Pattern Consistent with β-Thalassemia Trait Journal Articles
- A candidate transacting modulator of fetal hemoglobin gene expression in the Arab—Indian haplotype of sickle cell anemia Journal Articles
- A phased SNP-based classification of sickle cell anemia HBB haplotypes Journal Articles
- Characterization of Two Novel Deletions Involving the 5′ Region of the β-Globin Gene Journal Articles
- Editing aberrant splice sites efficiently restores β-globin expression in β-thalassemia Journal Articles
- Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype Journal Articles
- Hb North York [β117(G19)His→Asp]: A New β Chain Hemoglobin Variant Journal Articles
- Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family Journal Articles
- Hb S/ +-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the locus control region Journal Articles
- Hemoglobin Kenya composed of α‐ and (Aγβ)‐fusion‐globin chains, associated with hereditary persistence of fetal hemoglobin Journal Articles
- Identification of the first mutation in a BRE motif of the β-globin gene and its inheritance with two other α-globin gene mutations in a Lebanese family. Journal Articles
- Induced pluripotent stem cell–based mapping of β-globin expression throughout human erythropoietic development Journal Articles
- Mild β+-Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A) Journal Articles
- Molecular Characterization of a Novel 55.1 kbGγ(Aγδβ)0-thalassemia Deletion in Two Canadian Families Journal Articles
- New and Known β-Thalassemia Determinants Masked by Known and New δ Gene Defects [Hb A2-Ramallah or δ6(A3)Glu→Gln,GAG>>CAG] Journal Articles
- Newborn Screening for β-Thalassemia Identifies a Complex Genotype Involving a Novel β-Globin Gene Mutation ( HBB :c.336dup) Journal Articles
- Non-Thalassemic Phenotype Associated With the -83 (G > A) Mutation of theβ-Globin Gene Promoter (HBB: c.-133G > A) 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 High Oxygen Affinity Hemoglobin Variant in a Patient with Polycythemia: Hb Kennisis [β85(F1)Phe→Leu (TTT>TTG); HBB: c.258T>G] Journal Articles
- Severe fetal and neonatal hemolytic anemia due to a 198 kb deletion removing the complete β‐globin gene cluster Journal Articles
- Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients Journal Articles
- Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β 0 -Thalassemia Journal Articles
- Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion Journal Articles
- The First Report of a Homozygous Codons 9/10 (+T) β-Thalassemia Mutation in a Turkish Patient Journal Articles
- The genetics of hemoglobin A2 regulation in sickle cell anemia Journal Articles
- Three New β-Thalassemia Mutations with Varying Degrees of Severity Journal Articles
- Variants of ZBTB7A (LRF) and its β-globin gene cluster binding motifs in sickle cell anemia Journal Articles
- β 0 -Thalassemia Caused by a Novel Nonsense Mutation [ HBB: c.199A > T] Journal Articles
- β+-Thalassemia Trait Due to a Novel Mutation in the β-Globin Gene Promoter: −26 (A>C) [HBB c.−76A>C] Journal Articles