Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/49704
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dc.contributor.authorSakorn Pornpraserten_US
dc.contributor.authorThanatcha Wiengkumen_US
dc.contributor.authorSarinee Srithepen_US
dc.contributor.authorIsarapong Chainoien_US
dc.contributor.authorPanthong Singboottraen_US
dc.contributor.authorSanchai Wongwiwatthananukiten_US
dc.date.accessioned2018-09-04T04:05:47Z-
dc.date.available2018-09-04T04:05:47Z-
dc.date.issued2011-07-01en_US
dc.identifier.issn15986535en_US
dc.identifier.other2-s2.0-79961076404en_US
dc.identifier.other10.3343/kjlm.2011.31.3.138en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79961076404&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/49704-
dc.description.abstractBackground: Prevention and control of thalassemia requires simple, rapid, and accurate screening tests for carrier couples who are at risk of conceiving fetuses with severe thalassemia. Methods: Single-tube multiplex real-time PCR with SYBR Green1 and high-resolution melting (HRM) analysis were used for the identification of α-thalassemia-1 Southeast Asian (SEA) and Thai type deletions and β-thalassemia 3.5-kb gene deletion.The results were compared with those obtained using conventional gap-PCR. DNA samples were derived from 28 normal individuals, 11 individuals with α-thalassemia-1 SEA type deletion, 2 with α-thalassemia-1 Thai type deletion, and 2 with heterozygous β-thalassemia 3.5-kb gene deletion. Results: HRM analysis indicated that the amplified fragments from α-thalassemia-1 SEA type deletion, α-thalassemia-1 Thai type deletion, β-thalassemia 3.5-kb gene deletion, and the wild-type β-globin gene had specific peak heights at mean melting temperature (T m) values of 86.89°C, 85.66°C, 77.24°C, and 74.92°C, respectively. The results obtained using single-tube multiplex real-time PCR with SYBR Green1 and HRM analysis showed 100% consistency with those obtained using conventional gap-PCR. Conclusions: Single-tube multiplex real-time PCR with SYBR Green1 and HRM analysis is a potential alternative for routine clinical screening of the common types of α- and β-thalassemia large gene deletions, since it is simple, cost-effective, and highly accurate. © The Korean Society for Laboratory Medicine.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleDetection of α-thalassemia-1 Southeast Asian and Thai type deletions and β-thalassemia 3.5-kb deletion by single-tube multiplex real-time PCR with SYBR green 1 and high-resolution melting analysisen_US
dc.typeJournalen_US
article.title.sourcetitleKorean Journal of Laboratory Medicineen_US
article.volume31en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsLamphun Hospitalen_US
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