Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: prevalence and phenotypic analysis
Author:
Affiliation:
1. Department of Pediatrics, Faculty of Medicine; Khon Kaen University; Khon Kaen Thailand
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference7 articles.
1. Anion exchanger 1 mutations associated with distal renal tubular acidosis in the Thai population;Yenchitsomanus;J Hum Genet,2003
2. Neonatal hyperbilirubinemia associated with Southeast Asian ovalocytosis;Laosombat;Am J Hematol,1999
3. Molecular, hematological and clinical aspects of thalassemia major and thalassemia intermedia associated with Hb E-β-thalassemia in northeast Thailand;Nuntakarn;Blood Cells Mol Dis,2009
4. Coexistence of Southeast Asian ovalocytosis and beta-thalassemia: a molecular and hematological analysis;Fucharoen;Am J Hematol,2007
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1. Etiology and outcome of non-immune hydrops fetalis in relation to gestational age at diagnosis and intrauterine treatment;Journal of Perinatology;2021-09-06
2. Southeast Asian Ovalocytosis and Hemoglobinopathies in Newborns: Prevalence, Molecular, and Hematologic Analyses;Journal of Pediatric Hematology/Oncology;2020-08-18
3. Southeast asian ovalocytosis: the need for a carefull observation of red cell indices and blood smear;Annales de biologie clinique;2017-11
4. Concurrent β-thalassaemia trait and Southeast Asian ovalocytosis associated with clinically significant iron loading;Blood Cells, Molecules, and Diseases;2017-03
5. No Evidence for Role of Common Anion Exchanger 1 Mutations on the Severity Difference in HB E-β-Thalassemia Disease in Northeast Thailand;International Journal of Human Genetics;2013-06
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