alpha-Thalassemia Concept

subject area of

• A Multicenter Trial of the Effectiveness of ζ-Globin Enzyme-Linked Immunosorbent Assay and Hemoglobin H Inclusion Body Screening for the Detection of α⁰-Thalassemia Trait  Academic Article
• A Reliable Screening Test to Identify Adult Carriers of the (--SEA) alpha0-Thalassemia Deletion  Academic Article
• Allelic Stability of VNTR Locus 3’αHVR: Linkage Disequilibrium with the Common α-Thalassaemia-1-Deletion of South-East Asia (--SEA/)  Academic Article
• Alpha-thalassaemia and population health in Southeast Asia  Academic Article
• Anti-ζ Antibody Screening for α-Thalassemia Using Dried Filter Paper Blood  Academic Article
• Characterisation of the British α⁰-thalassaemia deletion: evidence of a founder effect in Newfoundland, Canada  Academic Article
• Characterization of a Rare Single α-Globin Gene Deletion in a Chinese Woman with Hb H Disease  Academic Article
• Codon 24 (TAT>TAG) and Codon 32 (ATG>AGG) (Hb Rotterdam): Two Novel α2 Gene Mutations Associated with Mild α-Thalassemia Found in the Same Family After Newborn Screening  Academic Article
• Coinheritance of α-thalassemia-1 and hemoglobin E/β0-thalassemia: Practical implications for neonatal screening and genetic counseling  Academic Article
• Comparison of haemoglobin H inclusion bodies with embryonic zeta globin in screening for alpha thalassaemia.  Academic Article
• Compromised genomic integrity impedes muscle growth after Atrx inactivation  Academic Article
• Consensus statement for the perinatal management of patients with α thalassemia major  Academic Article
• Detection of Severe Nondeletionalα-Thalassemia Mutations Using a Single-Tube Multiplex ARMS Assay  Academic Article
• Diagnostic Pitfall in PCR-Based α-Thalassemia Genotyping Resulting from a (G→C) Polymorphism at Nucleotide 71 3′ to the α2-Globin Gene Termination Codon  Academic Article
• Diagnostic testing for α‐globin gene disorders in a heterogeneous North American population  Academic Article
• Frameshift Mutation in the α2-Globin Gene Causing α⁺-Thalassemia: Codon 49 (−GC)  Academic Article
• Gigantic splenomegaly in a 27‐year‐old male of South‐East Asian descent with concurrent diagnosis of myeloproliferative neoplasm and hemoglobin H disease  Academic Article
• Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation  Academic Article
• Hb Evora [ 2 35, Ser->Pro], a novel hemoglobin variant associated with an  -thalassemia phenotype  Academic Article
• Hb H hydrops foetalis syndrome: a case report and review of literature  Academic Article
• Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases  Academic Article
• Hemoglobin H disease: not necessarily a benign disorder  Academic Article
• Hemoglobin H identification by high-performance liquid chromatography in confirmed hemoglobin H disease  Academic Article
• Hemoglobin SE Disease in Maine, and Severe Thalassemia in New Hampshire  Academic Article
• Hemoglobinopathies mimicking Hb S/β-thalassemia: Hb S/S with α-thalassemia and Hb S/Volga  Academic Article
• Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem  Academic Article
• IDENTIFICATION OF TWO NEW α-THALASSEMIA MUTATIONS IN EXON 2 OF THE α1-GLOBIN GENE  Academic Article
• Identification of a novel termination codon mutation (TAA-->TAT, Term-- >Tyr) in the alpha 2 globin gene of a Laotian girl with hemoglobin H disease [letter]  Academic Article
• Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome  Academic Article
• Immunocytological test to detect adult carriers of (--SEA/) deletional α-thalassaemia  Academic Article
• Limb defects in homozygous α-thalassemia: Report of three cases  Academic Article
• Microcytosis in patients with haemoglobin C trait: is α‐thalassaemia trait to blame?  Academic Article
• Multiple Minisequencing Screen for Seven Southeast Asian Nondeletional α-Thalassemia Mutations  Academic Article
• Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants  Academic Article
• Novel 27.9 kb α⁰-thalassemia deletion in a Filipino woman  Academic Article
• Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG orHBA1:c.2T>A)  Academic Article
• Novel Mutation of the α2-Globin Gene Initiation Codon (Atg→A-G) in a Vietnamese Girl with Hb H Disease  Academic Article
• PCR-based diagnosis of the Filipino (??FIL) and Thai (??THAI) ?-thalassemia-1 deletions  Academic Article
• Prevalence and Genotypes of α- and β-Thalassemia Carriers in Hong Kong — Implications for Population Screening  Academic Article
• Prevalence of Thalassemia in Patients With Microcytosis Referred for Hemoglobinopathy Investigation in Ontario  Academic Article
• Routine Screening of (--^SEA) α-Thalassemia Deletion by an Enzyme-Linked Immunosorbent Assay for Embryonic ζ-Globin Chains  Academic Article
• The alpha-globin gene cluster: genetics and disorders.  Academic Article
• The clinical significance of hemoglobinopathies in the Hamilton region: a twenty-year review  Academic Article
• The genetics of hemoglobin A₂regulation in sickle cell anemia  Academic Article
• Three New α-Thalassemia Point Mutations Ascertained Through Newborn Screening  Academic Article
• Two New α-Thalassemia Frameshift Mutations  Academic Article
• Universal Newborn Screening for Hb H Disease in California  Academic Article
• α-Thalassemia Caused by Two Novel Splice Mutations of the α2-Globin Gene: IVS-I-1 (G>A and G>T)  Academic Article
• α-Thalassemia: Hb H Disease and Hb Barts Hydrops Fetalis  Academic Article
• α⁺-Thalassemia Due to a Frameshift Mutation of theα2-Globin Gene [codons 55/56 (+T) orHBA2: c.168dup]  Academic Article
• α⁺-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT]  Academic Article
• α⁺-Thalassemia Trait Caused by a Nonsense Mutation in the α2-Globin Gene: Codon 54 (CAG>TAG)  Academic Article
• α⁰-Thalassemia Due to a 90.7 kb Deletion (– –^NFLD)  Academic Article