Blood · 2000 · 470 citations · 13 references
MedicineMolecular BiologyMolecular GeneticsMolecular DiagnosticsAnemiaSickle Cell DiseaseMultiplex Polymerase Chain Reaction (Pcr)
Alpha-thalassemia is very common throughout all tropical and subtropical regions of the world. In Southeast Asia and the Mediterranean regions, compound heterozygotes and homozygotes may have anemia that is mild to severe (hemoglobin [Hb] H disease) or lethal (Hb Bart's hydrops fetalis). We have developed a reliable, single-tube multiplex-polymerase chain reaction (PCR) assay for the 6 most frequently observed determinants of alpha-thalassemia. The assay allows simple, high throughput genetic screening for these common hematological disorders. (Blood. 2000;95:360-362)
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Cristiana Lo Nigro, Samuel S. Chong, Ann C. M. Smith et al. · Human Molecular Genetics · 1997 · 317 citations · Full text
The thalassemia syndromes: molecular basis and prenatal diagnosis in 1990.
H H Kazazian · PubMed · 1990 · 274 citations