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|dc.contributor.author||Delia C. Tang||en_US|
|dc.contributor.author||Griffin P. Rodgers||en_US|
|dc.contributor.other||National Institutes of Health, Bethesda||en_US|
|dc.contributor.other||The Institute of Science and Technology for Research and Development, Mahidol University||en_US|
|dc.contributor.other||National Institute of Diabetes and Digestive and Kidney Diseases||en_US|
|dc.identifier.citation||Journal of Laboratory and Clinical Medicine. Vol.137, No.4 (2001), 290-295||en_US|
|dc.description.abstract||The α-thalassemias are common genetic disorders that arise from reduced synthesis of the α-globin chains. At present, large-scale carrier screening and clinically valuable antenatal detection programs have not been established for the congenital disorder α-thalassemia (α-thal). We have developed a simple nonradioactive polymerase chain reaction (PCR) approach that can detect and differentiate several common α-globin gene deletional α-thals regardless of the break points. When three primer sets wereused - two gene-specific sets for the α1- and α2-globin genes and one set for the β-actin gene (serving as an internal control) - PCR products from genomic DNA were simultaneously amplified and analyzed after coamplification and gel electrophoresis. The number of α-globin genes present in the subjects was determined by the intensity of α1and α2bands normalized with that of β-actin when using densitometry. Our results demonstrate that five common genotypes of deletional α-thal are differentiated by the ratios of α1/β-actin and α2/β-actin. We also examined the feasibility of coupling this allele-specific amplification to a color-complementary assay. This easy and reproducible PCR assay is suitable for identifying α-thal carriers in screenings of large populations and improving genetic counseling.||en_US|
|dc.title||Rapid differentiation of five common α-thalassemia genotypes by polymerase chain reaction||en_US|
|Appears in Collections:||Scopus 2001-2005|
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