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 Journal Articles
- A Reliable Screening Test to Identify Adult Carriers of the (--SEA) alpha0-Thalassemia Deletion Journal Articles
- Allelic Stability of VNTR Locus 3’αHVR: Linkage Disequilibrium with the Common α-Thalassaemia-1-Deletion of South-East Asia (--SEA/) Journal Articles
- Alpha-thalassaemia and population health in Southeast Asia Journal Articles
- Anti-ζ Antibody Screening for α-Thalassemia Using Dried Filter Paper Blood Journal Articles
- Characterisation of the British α0‐thalassaemia deletion: evidence of a founder effect in Newfoundland, Canada Journal Articles
- Characterization of a Rare Single α-Globin Gene Deletion in a Chinese Woman with Hb H Disease Journal Articles
- 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 Journal Articles
- Coinheritance of α-thalassemia-1 and hemoglobin E/β0-thalassemia: Practical implications for neonatal screening and genetic counseling Journal Articles
- Comparison of haemoglobin H inclusion bodies with embryonic zeta globin in screening for alpha thalassaemia. Journal Articles
- Compromised genomic integrity impedes muscle growth after Atrx inactivation Journal Articles
- Consensus statement for the perinatal management of patients with α thalassemia major Journal Articles
- Detection of Severe Nondeletionalα-Thalassemia Mutations Using a Single-Tube Multiplex ARMS Assay Journal Articles
- 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 Journal Articles
- Diagnostic testing for α‐globin gene disorders in a heterogeneous North American population Journal Articles
- Frameshift Mutation in the α2-Globin Gene Causing α+-Thalassemia: Codon 49 (−GC) Journal Articles
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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 Journal Articles - Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype–phenotype correlation Journal Articles
- Hb Evora [ 2 35, Ser->Pro], a novel hemoglobin variant associated with an -thalassemia phenotype Journal Articles
- Hb H hydrops foetalis syndrome: a case report and review of literature Journal Articles
- Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases Journal Articles
- Hemoglobin H disease: not necessarily a benign disorder Journal Articles
- Hemoglobin H identification by high‐performance liquid chromatography in confirmed hemoglobin H disease Journal Articles
- Hemoglobin SE Disease in Maine, and Severe Thalassemia in New Hampshire Journal Articles
- Hemoglobinopathies mimicking Hb S/β‐thalassemia: Hb S/S with α‐thalassemia and Hb S/Volga Journal Articles
- Hydrops Fetalis Caused by α-Thalassemia: An Emerging Health Care Problem Journal Articles
- IDENTIFICATION OF TWO NEW α-THALASSEMIA MUTATIONS IN EXON 2 OF THE α1-GLOBIN GENE Journal Articles
- 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] Journal Articles
- Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome Journal Articles
- Immunocytological test to detect adult carriers of (--SEA/) deletional α-thalassaemia Journal Articles
- Limb defects in homozygous α-thalassemia: Report of three cases Journal Articles
- Microcytosis in patients with haemoglobin C trait: is α‐thalassaemia trait to blame? Journal Articles
- Multiple Minisequencing Screen for Seven Southeast Asian Nondeletional α-Thalassemia Mutations Journal Articles
- Mutations in the paralogous human α-globin genes yielding identical hemoglobin variants Journal Articles
- Novel 27.9 kb α0‐thalassemia deletion in a Filipino woman Journal Articles
- Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG orHBA1:c.2T>A) Journal Articles
- Novel Mutation of the α2-Globin Gene Initiation Codon (Atg→A-G) in a Vietnamese Girl with Hb H Disease Journal Articles
- PCR-based diagnosis of the Filipino (??FIL) and Thai (??THAI) ?-thalassemia-1 deletions Journal Articles
- Prevalence and Genotypes of α- and β-Thalassemia Carriers in Hong Kong — Implications for Population Screening Journal Articles
- Prevalence of Thalassemia in Patients With Microcytosis Referred for Hemoglobinopathy Investigation in Ontario Journal Articles
- Routine Screening of (--<sup>SEA</sup>) α-Thalassemia Deletion by an Enzyme-Linked Immunosorbent Assay for Embryonic ζ-Globin Chains Journal Articles
- The alpha-globin gene cluster: genetics and disorders. Journal Articles
- The clinical significance of hemoglobinopathies in the Hamilton region: a twenty-year review Journal Articles
- The genetics of hemoglobin A2 regulation in sickle cell anemia Journal Articles
- Three New α-Thalassemia Point Mutations Ascertained Through Newborn Screening Journal Articles
- Two New α-Thalassemia Frameshift Mutations Journal Articles
- Universal Newborn Screening for Hb H Disease in California Journal Articles
- α-Thalassemia Caused by Two Novel Splice Mutations of the α2-Globin Gene: IVS-I-1 (G>A and G>T) Journal Articles
- α+-Thalassemia Due to a Frameshift Mutation of theα2-Globin Gene [codons 55/56 (+T) orHBA2: c.168dup] Journal Articles
- α+-Thalassemia Trait Caused by a Frameshift Mutation in Exon 2 of the α2-Globin Gene [HBA2 c.244delT] Journal Articles
- α+-Thalassemia Trait Caused by a Nonsense Mutation in the α2-Globin Gene: Codon 54 (CAG>TAG) Journal Articles
- α0-Thalassemia Due to a 90.7 kb Deletion (– –NFLD) Journal Articles
- α‐Thalassemia: Hb H Disease and Hb Barts Hydrops Fetalis Journal Articles