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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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Samuel S. Chong
National University of Singapore
Corinne D. Boehm
Baylor College of Medicine
Douglas R. Higgs
University College Dublin
Blood
National University of Singapore
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Chong et al. (Sat,) studied this question.
synapsesocial.com/papers/69dad0ba78a3e0e288684767 — DOI: https://doi.org/10.1182/blood.v95.1.360
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