Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA<inf>2</inf> Levels on Capillary Electrophoresis

Diagnosis of Compound Heterozygous Hb Tak/β-Thalassemia and HbD-Punjab/β-Thalassemia by HbA<inf>2</inf> Levels on Capillary Electrophoresis

© 2017 Indian Society of Haematology & Transfusion Medicine A misdiagnosis of β-thalassemia carrier in samples with Hb Tak and HbD-Punjab, the β-variants, can be a cause of inappropriate genetic counseling thus having a new case of β-thalassemia major. A capillary electrophoresis (CE) is very...

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書目詳細資料
Main Authors:	Panyasai S., Sakkhachornphop S., Pornprasert S.
格式:	雜誌
出版:	2017
在線閱讀:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85017103358&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/40577
標簽:	添加標簽沒有標簽, 成為第一個標記此記錄!
機構:	Chiang Mai University

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