subject area of
- A new frameshift β°‐thalassemia mutation (codons 27–28 +C) found in a Chinese family Journal Articles
- A novel monoclonal antibody based diagnostic test for alpha-thalassemia- 1 carriers due to the (-SEA/) deletion Journal Articles
- A rapid and simple electrophoretic method for the detection of mutations involving small insertion or deletion: application to ?-thalassemia Journal Articles
- Changes in the Epidemiology of Thalassemia in North America: A New Minority Disease Journal Articles
- Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex. Journal Articles
-
Clinical phenotypes of three children with sickle cell disease caused by
HbS /Sicilian (δβ)0‐thalassemia deletion Journal Articles - Compound Heterozygosity For Triplicated α‐Globin Gene and (– –SEA) α‐Globin Gene Deletion: Implication For Thalassaemia Screening Journal Articles
- Compound Heterozygosity for two Genotypes of α-Thalassemia-2 : Hematological, Biosynthetic and DNA Studies Journal Articles
-
Detection of the (–
SEA ) double α‐globin gene deletion by a simple immunologic assay for embryonic ζ‐globin chains Journal Articles - Effect of Age at the Start of Iron Chelation Therapy on Gonadal Function in β-Thalassemia Major Journal Articles
- Embryonic ζ-Globin Chains in Adults: a Marker for α-Thalassemia-1 Haplotype Due to a >17.5-kb Deletion Journal Articles
- Haemoglobin D Los Angeles, D-β<sup>+</sup>-Thalassaemia, and D-β°- Thalassaemia 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/β°‐Thalassemia due to the ˜1.4‐kb deletion is associated with a relatively mild phenotype Journal Articles
- HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update Journal Articles
- HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server Journal Articles
- Hemoglobin Bart's Disease in an Italian Boy Journal Articles
- Hemoglobin E diseases: Hematological, analytical, and biosynthetic studies in homozygotes and double heterozygotes for α‐thalassemia Journal Articles
- Hemoglobin QIndia, α64(E l3) Asp→His, and β- Thalassemiaina Canadian Family Journal Articles
- Hemoglobin barts hydrops fetalis syndrome. Journal Articles
- Hemoglobinopathies in Canada Journal Articles
- High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene region. Journal Articles
- High hemoglobin A2 beta-thalassemia. Journal Articles
- Human embryonic zeta-globin chain expression in deletional alpha- thalassemias Journal Articles
- Human embryonic zeta-globin chains in adult patients with alpha-thalassemias. Journal Articles
- Identification of an extensive ζ‐α globin gene deletion in a Chinese individual Journal Articles
- Identification of hemoglobin E by the isopropanol solubility test 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
- Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies Journal Articles
- Laboratory diagnosis of HB CC-α-thalassemia Journal Articles
- Molecular Characterization of a Novel 55.1 kbGγ(Aγδβ)0-thalassemia Deletion in Two Canadian Families Journal Articles
- Non-Thalassemic Phenotype Associated With the -83 (G > A) Mutation of theβ-Globin Gene Promoter (HBB: c.-133G > A) Journal Articles
- Perspectives on anemia: Factors confounding understanding of past occurrence Journal Articles
- Positional effect of cis/trans alpha globin gene deletions on the formation of “H” bodies Journal Articles
- Potential Application of a New Screening Test for α-Thalassemia-1 Carriers Journal Articles
- Prenatal Diagnosis of Hemoglobinopathies in Ontario, Canada Journal Articles
- Presacral extramedullary hematopoiesis in thalassemia intermedia. Journal Articles
- Proficiency Testing of Hemoglobinopathy Techniques in Ontario Laboratories Journal Articles
- Second Report of Hb Toulon [α77(EF6)Pro→His] in a Canadian Family of Italian Descent Journal Articles
- Should we screen for globin gene mutations in blood samples with mean corpuscular volume (MCV) greater than 80 fL in areas with a high prevalence of thalassaemia? Journal Articles
- Sickle Cell Traits in Canada Journal Articles
- The Interaction of Anti 3. 7 Type Quadruplicated α-Globin Genes and Heterozygous β-Thalassemia Journal Articles
- The Intrauterine Diagnosis of Hemoglobin Disorders Journal Articles
- The T----C substitution at nucleotide + 1570 of the beta-globin gene is a polymorphism [letter; comment] Journal Articles
- The clinical severity of hemoglobin S/Black (Aγδβ)0‐thalassemia Journal Articles
- The thalassemias and health care in Canada: a place for genetics in medicine. Journal Articles
- Two novel beta-thalassemia mutations in the 5' and 3' noncoding regions of the beta-globin gene [see comments] Journal Articles
- β‐thalassemia intermedia caused by compound heterozygosity for Hb Malay (β codon 19 AAC→AGC; Asn→Ser) and codons 41/42 (‐CTTT) β 0 ‐thalassemia mutation Journal Articles
- δβ-Thalassemia in an African-American: Identification of the deletion endpoints and PCR-Based diagnosis Journal Articles