subject area of
- Characterisation of the British α0‐thalassaemia deletion: evidence of a founder effect in Newfoundland, Canada 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
- Diagnostic testing for α‐globin gene disorders in a heterogeneous North American population Journal Articles
- Fetal globin gene inducers: novel agents and new potential 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
- Hemoglobin H identification by high‐performance liquid chromatography in confirmed hemoglobin H disease 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
- 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
- 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