subject area of
- A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells Journal Articles
- A Novel Sickle Hemoglobin: Hemoglobin S-South End Journal Articles
- A Novel Sickling Hemoglobinopathy Journal Articles
- Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin kenya Journal Articles
- Compound Heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (Aγ81Leu-β86Ala) in a Ugandan Woman Journal Articles
- Compound Heterozygosity for Hb S and Hb G-Copenhagen Journal Articles
- DNA diagnosis of Hb S and Hb Caribbean (α2β291 Leu→Arg) in a Jamaican family Journal Articles
- Evidence for a mechanosensitive calcium influx into red cells Journal Articles
- Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin Journal Articles
- Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype Journal Articles
- Fetal hemoglobin in sickle cell anemia: a glass half full? Journal Articles
- Genetic studies of fetal hemoglobin in the Arab‐Indian haplotype sickle cell‐β0 thalassemia Journal Articles
- Hb Hope [β136(H14)Gly→Asp (GGT→GAT)]: Interactions with Hb S [β6(A3)Glu→Val (GAG→GTG)], Other Variant Hemoglobins and Thalassemia 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
- Hb S/β°‐Thalassemia due to the ˜1.4‐kb deletion is associated with a relatively mild phenotype Journal Articles
- Hemoglobin SE Disease in Maine, and Severe Thalassemia in New Hampshire Journal Articles
- Hemoglobin SE disease—A concise review Journal Articles
- Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease Journal Articles
- High Hb A2β-Thalassemia Due to a 468 bp Deletion in a Patient with Hb S/β-Thalassemia Journal Articles
- Longitudinal Decline in Lung Volume in a Population of Children with Sickle Cell Disease Journal Articles
- Massive splenic infarction in an adolescent with hemoglobin S‐HPFH Journal Articles
- Non-Thalassemic Phenotype Associated With the -83 (G > A) Mutation of theβ-Globin Gene Promoter (HBB: c.-133G > A) Journal Articles
- Optimal Manual Exchange Transfusion Protocol for Sickle Cell Disease: A Retrospective Comparison of Two Comprehensive Care Centers in the United Kingdom and Canada Journal Articles
- Proficiency Testing of Hemoglobinopathy Techniques in Ontario Laboratories Journal Articles
- Sickle Cell Traits in Canada Journal Articles
- Sickle cell disease caused by Hb S/Québec‐CHORI: Treatment with hydroxyurea and response Journal Articles
- Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients Journal Articles
- Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7‐kb β‐globin gene deletion Journal Articles
- Splice Acceptor Mutation [ HBB :c.93-2A > T] in a Patient with Hb S/β 0 -Thalassemia Journal Articles
- Stuttering priapism in a patient with sickle cell trait treated with automated red cell exchange transfusion Journal Articles
- THE Hb S/β+-Thalassemia Phenotype Demonstrates that the IVS-I (−2) (A>C) Mutation is a Mild β-Thalassemia Allele Journal Articles
- The Intrauterine Diagnosis of Hemoglobin Disorders Journal Articles
- The clinical severity of hemoglobin S/Black (Aγδβ)0‐thalassemia Journal Articles
- The genetics of hemoglobin A2 regulation in sickle cell anemia Journal Articles
- Three New β-Globin Gene Promoter Mutations Identified Through Newborn Screening Journal Articles