Abnormal processing of β-Malay globin RNA
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference27 articles.
1. Molecular basis and prenatal diagnosis of beta-thalassemia
2. Molecular characterization of β-globin gene mutations in Malay patients with Hb E-β-thalassaemia and thalassaemia major
3. Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes
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1. Hemoglobinopathy Screening in a 15-Year-old Patient With Anemia;Journal of Pediatric Hematology/Oncology;2015-08
2. A large cohort of β+-thalassemia in Thailand: Molecular, hematological and diagnostic considerations;Blood Cells, Molecules, and Diseases;2015-02
3. Presumptive diagnosis of common haemoglobinopathies in Southeast Asia using a capillary electrophoresis system;International Journal of Laboratory Hematology;2011-02-22
4. Compound heterozygote states for Hb C/Hb Malay and Hb C/Hb E in pregnancy: A molecular and hematological analysis;Blood Cells, Molecules, and Diseases;2005-09
5. β‐thalassemia intermedia caused by compound heterozygosity for Hb Malay (β codon 19 AAC→AGC; Asn→Ser) and codons 41/42 (‐CTTT) β 0 ‐thalassemia mutation;American Journal of Hematology;2000-06-15
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