Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/52173
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dc.contributor.authorSakorn Pornpraserten_US
dc.contributor.authorManoo Punyamungen_US
dc.contributor.authorKallayanee Treesuwanen_US
dc.date.accessioned2018-09-04T09:21:45Z-
dc.date.available2018-09-04T09:21:45Z-
dc.date.issued2013-12-01en_US
dc.identifier.issn14336510en_US
dc.identifier.other2-s2.0-84891600436en_US
dc.identifier.other10.7754/Clin.Lab.2013.121217en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84891600436&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/52173-
dc.description.abstractBackground: Using a single tube multiplex real-time PCR with SYBR Greenl and high resolution melting (HRM) analysis in routine laboratory for detection of α-thalassemia-1 Southeast Asian (SEA) type deletion simultaneously with Thai type deletion is costly. Methods: Criteria for laboratory testing of α-thalassemia-1 Thai type deletion were set as follow: (1) MCV ≤ 75 fL and negative for α-thalassemia-1 SEA type deletion, β-thalassemia or homozygous HbE; (2) HbE trait with HbE level < 21.5% and negative for α-thalassemia-1 SEA type deletion; or (3) Hb Bart's and HbH found on HPLC chromatogram but negative for α-thalassemia-1 SEA type deletion. Results: From May 2010 to October 2012, the number of samples to detect for α-thalassemia-1 Thai type deletion decreased from 15,081 to 672 samples and the α-thalassemia-1 Thai type deletion trait was found in 7 samples (1.04%). Conclusions: The new testing algorithm can reduce number of samples for detection of α-thalassemia-1 Thai type deletion.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleCriteria for detection of α-Thalassemia-1 Thai type deletion in routine laboratoryen_US
dc.typeJournalen_US
article.title.sourcetitleClinical Laboratoryen_US
article.volume59en_US
article.stream.affiliationsChiang Mai Universityen_US
Appears in Collections:CMUL: Journal Articles

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