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
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Gigantic splenomegaly in a 27‐year‐old male of
S outh‐E astA sian descent with concurrent diagnosis of myeloproliferative neoplasm and hemoglobinH 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 (--<sup>SEA</sup>) 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