Unusual phenotype of Hemoglobin EE with Hemoglobin H disease: a pitfall in clinical diagnosis and genetic counseling
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference12 articles.
1. Hemoglobinopathies in Southeast Asia: molecular biology and clinical medicine;Fucharoen;Hemoglobin,1997
2. Alpha- and beta-thalassemia in Thailand;Wasi;Ann N Y Acad Sci,1969
3. EF Bart's disease: interaction of the abnormal alpha- and beta-globin genes;Fucharoen;Eur J Haematol,1988
4. Hemoglobin E disorders;Fucharoen,2001
5. Perentesis JP Coinheritance of a-thalassemia-1 and hemoglobin E/b0-thalassemia: practical implications for neonatal screening and genetic counseling;Krishnamurti;J Pediatr,1998
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots;Annals of Clinical Biochemistry: International Journal of Laboratory Medicine;2013-07-30
2. Detection of Hb E mutation (β26, GAG-AAG, Glu-Lys) using allelic discrimination analysis;International Journal of Laboratory Hematology;2009-01-11
3. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: A molecular and hematological analysis;Blood Cells, Molecules, and Diseases;2007-09
4. Molecular and hematological profiles of hemoglobin EE disease with different forms of α-thalassemia;Annals of Hematology;2006-03-25
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