Two thalassemia intermedia patients with δβ/β-thalassemia and a deletional type α-thalassemia [7]

Haematologica

Volumn 86, Issue 1, 2001, Pages 108-

  Li, Z ^a   Liu, L ^a   Zhao, Y ^a   Zhong, X ^a   Xu, X ^a  

^a SOUTHERN MEDICAL UNIVERSITY   (China)

Author keywords

Genotype; Phenotype; Thalassemia intermedia

Indexed keywords

ADOLESCENT; ALPHA THALASSEMIA; BETA THALASSEMIA; CASE REPORT; CHINESE; FEMALE; GENE DELETION; GENOTYPE; HETEROZYGOSITY; HUMAN; HUMAN CELL; HUMAN TISSUE; LETTER; MALE; PHENOTYPE; THALASSEMIA INTERMEDIA;

ADOLESCENT; ADULT; ALPHA-THALASSEMIA; ASIA, SOUTHEASTERN; BETA-THALASSEMIA; CHINA; FAMILY HEALTH; FEMALE; GENOTYPE; HUMANS; MALE; MIDDLE AGED; MUTATION; PHENOTYPE; THALASSEMIA;

EID: 0035136908     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (8)

1. The thalassemias related disorders: Quantitative disorders of hemoglobin synthesis
2. Relationship between genotype and phenotype. Thalassemia intermedia
3. Thalassemia intermedia
4. Delta beta thalassemia and hereditary persistence of fetal hemoglobin
5. Delta-beta-thalassaemia in a Chinese family
6. O thalassemia
7. O thalassemia deletion: Comparison to other deletions in the human beta-globin gene cluster and sequence analysis of the breakpoints
8. The molecular basis of HPFH and β-thalassemia in Chinese population