Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/62406
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dc.contributor.authorOrathai Tangvarasittichaien_US
dc.contributor.authorChanthonrat Sitthiworananen_US
dc.contributor.authorWarong Dechgitvigromen_US
dc.contributor.authorTorpong Sanguansermsrien_US
dc.contributor.authorRattima Jeenapongsaen_US
dc.date.accessioned2018-09-11T09:26:53Z-
dc.date.available2018-09-11T09:26:53Z-
dc.date.issued2005-04-01en_US
dc.identifier.issn11082682en_US
dc.identifier.other2-s2.0-21744458323en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=21744458323&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/62406-
dc.description.abstractThe prevalence, molecular characteristics and haematological study of thalassaemia in lower northern Thailand were determined in 1,000 pregnant women who attended an antenatal clinic at Buddhachinaraj Hospital, Phitsanulok, Thailand. A complete blood count, Hb A2 quantification and DNA analysis were performed. The results exhibit the prevalence of α10-thalassaemia, α+-thalassaemia and β-thalassaemia as 5.3%, 14.6%, and 1.4%, respectively. Regarding the abnormal haemoglobins, the prevalence of HbE, Hb Constant Spring (CS), and Hb Pakse (PS) was 24.2%, 5.3%, and 0.1%, respectively. MCV and MCH were significantly different between thalassaemia carriers and normal subjects. Since the MCV of less than 75 fl and MCH of less than 25 pg were found in all α0-thalassaemia subjects, these parameters could be used for α0-thalassaemia screening. Copyright © Hellenic Society of Haematology.en_US
dc.subjectMedicineen_US
dc.titlePrevalence and haematological parameters of thalassaemia in Lower Northern Thailanden_US
dc.typeJournalen_US
article.title.sourcetitleHAEMAen_US
article.volume8en_US
article.stream.affiliationsNaresuan Universityen_US
article.stream.affiliationsBuddhachinaraj Hospitalen_US
article.stream.affiliationsChiang Mai Universityen_US
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