Abstract
The strategy for early prenatal diagnosis of β-thalassemia in Singapore by direct detection of the mutant β-globin gene requires the spectrum of mutations producing the disorder in this population to be characterized. We analyzed 134 β-thalassemia alleles from Singapore by specific oligonucleotide hybridization after DNA amplification, using a nonradioactive enhanced chemiluminescence detection system. The mutations were identified in 90% of the alleles using five oligonucleotide probes for the following mutations: codons 41/42 (deletion -TCTT), IVS II nt 654 (C→T), codon 17 (A→T), IVS I nt 5 (G→C), and -28 TATA box (A→G). Together with the strategy of direct sequencing, a total of 97% of the mutations were identified. In the Chinese subpopulation, 97% of the mutations were detected by the oligonucleotide probes. Using just four oligonucleotide probes would identify 96% of the mutations, and 76% of the mutations were accounted for by codon 41/42 (-TCTT) and IVS II nt 654 (C→T) mutations. Thus in this subpopulation early prenatal diagnosis would be possible in virtually all the affected families.
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Ng, I.S.L., Ong, J.B.K., Tan, C.L. et al. β-Thalassemia mutations in Singapore — a strategy for prenatal diagnosis. Hum Genet 94, 385–388 (1994). https://doi.org/10.1007/BF00201598
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DOI: https://doi.org/10.1007/BF00201598