Phenotypic prediction in β-thalassemia

Annals of the New York Academy of Sciences

Volumn 850, Issue , 1998, Pages 436-441

  Ho, P J ^a,c   Hall, G W ^a   Luo, L Y ^a   Weatherall, D J ^a   Thein, S L ^a,b  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^c ROYAL PRINCE ALFRED HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

BETA GLOBIN;

BETA THALASSEMIA; CONFERENCE PAPER; DISEASE SEVERITY; GENE FREQUENCY; GENOTYPE; GLOBIN GENE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; PHENOTYPE;

EID: 0031824743     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1998.tb10514.x     Document Type: Conference Paper

References (6)

1. BAYSAL, E. et al. 1995. The β- and δ-thalassemia repository. Hemoglobin 19: 213-236.
2. WEATHERALL, D. J. et al. 1981. The Thalassaemia Syndromes. Blackwell Scientific. Oxford.
3. THEIN, S. L. 1993. β-thalassaemia. Baillière's Clin. Haematol. 6: 151-176. London.
4. SHARPE, J. A. et al. 1989. Haemoglobin analysis. In Laboratory Haematology, Chanarin, Ed. 1: 33-54. Churchill Livingstone. Edinburgh.
5. THEIN, S. L. et al. 1993. β-thalassemia unlinked to the β-globin gene in an English family. Blood 82: 961-967.
6. CRAIG, J. E. et al. 1993. The molecular basis of HPFH in a British family identified by heteroduplex formation. Br. J. Haematol. 84: 106-110.