Molecular analysis of a Thai β-thalassaemia heterozygote with normal haemoglobin A2 level: Implication for population screening

Annals of Clinical Biochemistry

Volumn 39, Issue 1, 2002, Pages 44-49

  Fucharoen, S ^a   Fucharoen, G ^a   Sanchaisuriya, K ^a   Pengjam, Y ^a  

^a KHON KAEN UNIVERSITY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

2,6 DICHLOROPHENOLINDOPHENOL; ALPHA GLOBIN; BETA GLOBIN; CELLULOSE ACETATE; HEMOGLOBIN A; HEMOGLOBIN A2; HEMOGLOBIN E;

ADULT; ALLELE; ARTICLE; BETA THALASSEMIA; CASE REPORT; CODON; DISEASE SEVERITY; ELECTROPHORESIS; FEMALE; GENE DELETION; GENOTYPE; HEMOGLOBIN DETERMINATION; HEMOGLOBINOPATHY; HETEROZYGOSITY; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; MASS SCREENING; MOLECULAR BIOLOGY; OSMOTIC FRAGILITY; POLYMERASE CHAIN REACTION; POPULATION RISK; PRIORITY JOURNAL; SCREENING TEST; THAILAND; THALASSEMIA;

ADULT; ALPHA-THALASSEMIA; BETA-THALASSEMIA; DNA; DNA PRIMERS; FEMALE; GENE DELETION; GLOBINS; HEMOGLOBIN A2; HETEROZYGOTE; HUMANS; MASS SCREENING; MOLECULAR BIOLOGY; POLYMERASE CHAIN REACTION; THAILAND;

EID: 0036153972     PISSN: 00045632     EISSN: None     Source Type: Journal    
DOI: 10.1258/0004563021901720     Document Type: Article

References (24)

1. Thalassaemia in Thailand
2. 2: Origin, evolution and aftermath
3. Effectiveness of one tube osmotic fragility screening in detecting β-thalassaemia trait
4. Haemoglobin E, an oxidatively unstable mutation
5. Solid-phase enzyme immunoassay for serum ferritin
6. Haemoglobin analysis
7. Molecular basis of β-thalassaemia in Thailand: Analysis of β-thalassaemia mutations using the polymerase chain reaction
8. Molecular analysis of globin genes: Application to prenatal diagnosis of thalassaemia
9. A simple non radioactive method for detecting β-thalassaemia/HbE disease: Application to prenatal diagnosis
10. Rapid and simultaneous non-radioactive method for detecting α-thalassaemia 1 (SEA type) and Hb Constant Spring genes
11. The molecular basis of α-thalassaemia in Thailand
12. δ-Thalassaemia caused by disruption of the site for an erythroid specific transcription factor, GATA-1 in the δ-globin gene promotor
13. Generation and spread of globin mutations in populations: β-thalassaemia in Asian countries
14. Prenatal diagnosis of thalassaemia and haemoglobinopathies in Thailand: Experience from 100 pregnancies
15. 2 in patients with different β-thalassaemia mutations and a δ-chain variant
16. 2 levels: Implication for β-thalassaemia carrier screening
17. 2 β-thalassaemia
18. 2 levels
19. 2 and E
20. 2 in iron deficient β-thalassaemia heterozygotes
21. The risk of α-thalassaemia in offspring of β-thalassaemia carriers in Hong Kong
22. β-Thalassaemia with α-thalassaemia in Thailand
23. The thalassaemia working party of the BCSH general haematology task force. Guidelines for investigation of the α- and β-thalassaemia traits