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Co-inheritance of α0 -thalassemia elevates Hb A2 level in homozygous Hb E: Diagnostic implications.
Singha, K; Srivorakun, H; Fucharoen, G; Fucharoen, S.
Affiliation
  • Singha K; Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.
  • Srivorakun H; Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.
  • Fucharoen G; Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.
  • Fucharoen S; Centre for Research and Development of Medical Diagnostic Laboratories, Faculty of Associated Medical Sciences, Khon Kaen University, Khon Kaen, Thailand.
Int J Lab Hematol ; 39(5): 508-512, 2017 Oct.
Article in En | MEDLINE | ID: mdl-28497611
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hemoglobin A2 / Hemoglobin E / Alpha-Thalassemia / Inheritance Patterns / Homozygote Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Int J Lab Hematol Journal subject: HEMATOLOGIA Year: 2017 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hemoglobin A2 / Hemoglobin E / Alpha-Thalassemia / Inheritance Patterns / Homozygote Type of study: Diagnostic_studies / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Int J Lab Hematol Journal subject: HEMATOLOGIA Year: 2017 Document type: Article Affiliation country: