Simple method for screening of α-thalassaemia 1 carriers
α-Thalassaemia 1 genetic disorder occurs when there is a deletion of two linked α-globin genes. The interaction between these abnormal genes leads to the most severe type of thalassaemia disease, haemoglobin (Hb) Bart's hydrops fetalis. The identification of α-thalassaemia 1 carriers and geneti...
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| Main Authors: | , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
2014
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| Online Access: | http://www.scopus.com/inward/record.url?eid=2-s2.0-67749088035&partnerID=40&md5=2621fa1b89d8cdb0af28960e4196c93b http://cmuir.cmu.ac.th/handle/6653943832/773 |
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| Institution: | Chiang Mai University |
| Language: | English |