Identification of α-thalassemia mutations in Iranian individuals with abnormal hematological indices and normal Hb A2

Hemoglobin

Volumn 27, Issue 2, 2003, Pages 129-132

  Gohari, Ladan H ^a   Petrou, Miranda ^b   Felekis, Xenia ^b   Christopoulos, George ^b   Kleanthous, Marina ^b  

^a IRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^b CYPRUS INSTITUTE OF NEUROLOGY AND GENETICS   (Cyprus)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN A2;

ALLELE; ALPHA THALASSEMIA; AMINO ACID SUBSTITUTION; ARTICLE; DNA DETERMINATION; FEMALE; GENE MUTATION; GENE SEQUENCE; GENOTYPE; HUMAN; IRAN; MAJOR CLINICAL STUDY; MALE; POLYADENYLATION; POLYMERASE CHAIN REACTION;

ALPHA-THALASSEMIA; BASE SEQUENCE; DNA PRIMERS; FEMALE; GENOTYPE; HEMOGLOBIN A2; HUMANS; IRAN; MALE; MUTATION; POLYMERASE CHAIN REACTION; RESTRICTION MAPPING;

IRANIA;

EID: 0038585073     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.1081/HEM-120021548     Document Type: Article

References (3)

1. Thalassemia prevention program in Iran. TIF Magazine 2002; 35:13-15.
2. Liu YT, Old JM, Miles K, Fisher CA, Weatherall DJ, Clegg JB. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol 2002; 108:295-299.
3. Kyriacou K, Kyrri A, Kalogirou E, Vasiliades P, Angastiniotis M, Ioannou PA, Kleanthous M. Hb Bart's levels in cord blood and α-thalassemia mutations in Cyprus. Hemoglobin 2000; 24(3):171-180.