Complex Interaction of Hb E [β26(B8)Glu→Lys], Hb Korle-Bu [β73(E17)Asp→Asn] and a Deletional α-thalassemia-1 in Pregnancy
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630260903343780
Reference21 articles.
1. Hemoglobinopathies in Southeast Asia
2. Atypical hemoglobin H disease in a Thai patient resulting from a combination of α-thalassemia 1 and hemoglobin Constant Spring with hemoglobin J Bangkok heterozygosity
3. Complex interaction of Hb Hekinan [α27(B8) Glu-Asp] and Hb E [β26(B8) Glu-Lys] with a deletional α-thalassemia 1 in a Thai family
4. Triple Heterozygosity of a Hemoglobin Variant: Hemoglobin Pyrgos With Other Hemoglobinopathies
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1. A Unique Case of a Compound Heterozygosity of Hemoglobin Korle-Bu and Sickle Cell Trait in a Military Trainee;Journal of Hematology;2024-06
2. Frequency of unnecessary prenatal diagnosis of hemoglobinopathies: A large retrospective analysis and implication to improvement of the control program;PLOS ONE;2023-04-14
3. A Large Cohort of Hemoglobin Variants in Thailand: Molecular Epidemiological Study and Diagnostic Consideration;PLoS ONE;2014-09-22
4. Incidence of haemoglobin E and α-thalassaemia mutations and their interaction among the tribal populations of Assam and Arunachal Pradesh in North Eastern India;The Nucleus;2013-07-17
5. Hb Phimai [β72(E16)Ser→Thr]: A Novel β-Globin Structural Variant Found in Association with Hb Constant Spring in Pregnancy;Hemoglobin;2011-03-21
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