subject area of
- A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells Academic Article
- A Novel Sickle Hemoglobin: Hemoglobin S-South End Academic Article
- A Novel Sickling Hemoglobinopathy Academic Article
- Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin kenya Academic Article
- Compound Heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (Aγ81Leu-β86Ala) in a Ugandan Woman Academic Article
- Compound Heterozygosity for Hb S and Hb G-Copenhagen Academic Article
- DNA diagnosis of Hb S and Hb Caribbean (α2β291 Leu→Arg) in a Jamaican family Academic Article
- Evidence for a mechanosensitive calcium influx into red cells Academic Article
- Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin Academic Article
- Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype Academic Article
- Fetal hemoglobin in sickle cell anemia: a glass half full? Academic Article
- Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-β0thalassemia Academic Article
- Hb Hope [β136(H14)Gly→Asp (GGT→GAT)]: Interactions with Hb S [β6(A3)Glu→Val (GAG→GTG)], Other Variant Hemoglobins and Thalassemia Academic Article
- Hb S/ +-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the locus control region Academic Article
- Hb S/β°-Thalassemia due to the ˜1.4-kb deletion is associated with a relatively mild phenotype Academic Article
- Hemoglobin SE Disease in Maine, and Severe Thalassemia in New Hampshire Academic Article
- Hemoglobin SE disease—A concise review Academic Article
- Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease Academic Article
- High Hb A2β-Thalassemia Due to a 468 bp Deletion in a Patient with Hb S/β-Thalassemia Academic Article
- Longitudinal Decline in Lung Volume in a Population of Children with Sickle Cell Disease Academic Article
- Massive splenic infarction in an adolescent with hemoglobin S-HPFH Academic Article
- Non-Thalassemic Phenotype Associated With the -83 (G > A) Mutation of theβ-Globin Gene Promoter (HBB: c.-133G > A) Academic Article
- Optimal Manual Exchange Transfusion Protocol for Sickle Cell Disease: A Retrospective Comparison of Two Comprehensive Care Centers in the United Kingdom and Canada Academic Article
- Proficiency Testing of Hemoglobinopathy Techniques in Ontario Laboratories Academic Article
- Sickle Cell Traits in Canada Academic Article
- Sickle cell disease caused by Hb S/Québec-CHORI: Treatment with hydroxyurea and response Academic Article
- Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients Academic Article
- Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb ?-globin gene deletion Academic Article
- THE Hb S/β+-Thalassemia Phenotype Demonstrates that the IVS-I (−2) (A>C) Mutation is a Mild β-Thalassemia Allele Academic Article
- The Intrauterine Diagnosis of Hemoglobin Disorders Academic Article
- The clinical severity of hemoglobin S/Black (A γδβ)0 -thalassemia Academic Article
- The genetics of hemoglobin A2regulation in sickle cell anemia Academic Article
- Three New β-Globin Gene Promoter Mutations Identified Through Newborn Screening Academic Article