Molecular spectrum of β-thalassemia in the Iranian Province of Hormozgan

Hemoglobin

Volumn 25, Issue 1, 2001, Pages 35-43

  Yavarian, M ^a   Harteveld, C L ^a   Batelaan, D ^a   Bernini, L F ^a   Giordano, P C ^a  

^a LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

5' UNTRANSLATED REGION; ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; BETA THALASSEMIA; DENATURING GRADIENT GEL ELECTROPHORESIS; GENE FREQUENCY; GENE MUTATION; HETEROZYGOTE; HIGH RISK POPULATION; HOMOZYGOSITY; HUMAN; IRAN; MAJOR CLINICAL STUDY; NETHERLANDS; PHENOTYPE; SEQUENCE ANALYSIS;

5' UNTRANSLATED REGIONS; ALLELES; AMINO ACID SUBSTITUTION; BETA-THALASSEMIA; CLUSTER ANALYSIS; DNA MUTATIONAL ANALYSIS; ETHNIC GROUPS; GENE FREQUENCY; GENOTYPE; GLOBINS; HETEROZYGOTE DETECTION; HUMANS; IRAN; MUTATION, MISSENSE; NETHERLANDS; POLYMERASE CHAIN REACTION; SEQUENCE DELETION;

IRANIA;

EID: 0035091652     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.1081/HEM-100103068     Document Type: Article

References (16)

1. Clinical experience of management of thalassaemia: The Sardinian experience
2. The molecular spectrum of β-thalassemia and abnormal hemoglobins in the allochthonous and autochthonous Dutch population
3. Denaturing gradient gel electrophoresis and direct sequencing of PCR amplified genomic DNA: A rapid and reliable diagnostic approach to β-thalassaemia
4. β-thalassaemia
5. Two novel β-thalassemia mutations in the 5′ and 3′ non-coding regions of the β-globin gene
6. A C → T substitution at nt - 101 in a conserved DNA sequence of the promotor region of the β-globin gene is associated with "silent" β-thalassemia
7. Molecular analyses of β-thalassemia in Iran
8. β-thalassemia in Iran: A high incidence of the nonsense codon 39 mutation on the island of Queshem
9. Prevention of hemoglobinopathies in The Netherlands: An individual approach based on information and prospective diagnostics
10. Evaluation of the BeTha Gene 1 kit for the qualitative detection of the eight most common Mediterranean β-thalassemia mutations
11. β-globin gene mutations among β-thalassemic patients from Boushehr province in south of Iran
12. β-globin gene mutation frequencies in 104 thalassaemic patients from Khouezestan Province in Southwest of Iran
13. IVS-I nt5 mutation accounts for 68.9% of β-thalassemia patients from Sistan-Balouchestan in Southeast of Iran
14. IVS-II nt 1 mutation accounts for nearly 51% of β-globin gene mutations in Tehran province
15. β-thalassemia in Southwestern Iran