References
- Higgs D R. α-Thalassaemia. Bailliere's Clin Haematol 1993; 6(1):117–150, [CSA]
- Harteveld C L, van Delft P, Plug R, Versteegh F GA, Hagen B, van Rooijen I, Kok P JMJ, Wajcman H, Kister J, Giordano P C. Hb Groene Hart: a new Pro→Ser amino acid substitution at position 119 of the α1-globin chain is associated with a mild α-thalassemia phenotype. Hemoglobin 2002; 26(3):255–260, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Papassotiriou I, Traeger-Syndinos J, Vlachou C, Karagiorga M, Metaxotou A, Kanavakis E, Stamoulakatou A. Rapid and accurate quantitation of Hb Bart's and Hb H using weak cation exchange high performance liquid chromatography: correlation with the α-thalassemia genotype. Hemoglobin 1999; 23(3):203–211, [PUBMED], [INFOTRIEVE], [CSA]
- Liu Y T, Old J M, Miles K, Fisher C A, Weatherall D J, Clegg J B. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multipex polymerase chain reactions. Br J Haematol 2000; 108(2):295–299, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Bowden D K, Vickers M A, Higgs D R. A PCR-based strategy to detect the common severe determinants of α-thalassaemia. Br J Haematol 1992; 84(1):104–108, [CSA]
- Jassim N, Al-Arrayed S, Gerard N, Al-Mukharraq H, Al-Ajami A, Ramasawmy R, Krishnamoorthy R. A mismatched-primer polymerase chain reaction–restriction fragment length polymorphism strategy for rapid screening of the polyadenylation signal mutation αT-Saudi (AATAAA→AATAAG) in the α2-globin gene. Hemoglobin 1999; 23(3):213–220, [PUBMED], [INFOTRIEVE], [CSA]
- Ayala S, Colomer D, Aymeirich M, Vives Corrons J LI. Non deletional α-thalassemia first description of αHphIα and αNcoIα mutations in Spanish population. Am J Hematol 1996; 52(3):144–149, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Siala H, Fattoum S, Messaoud T, Ouali, Gerard N, Krishnamoorthy R. A novel α-thalassemia nonsense mutation in codon 23 of the α2-globin gene (GAG→TAG) in a Tunisian family. Hemoglobin 2004; 28(3):249–254, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Harteveld K L, Heister A JGAM, Giordano P C, Losekoot M, Bernini L F. Rapid detection of point mutations and polymorphisms of α-globin genes by DGGE and SSCA. Hum Mutat 1996; 7(2):114–122, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Traeger-Synodinos J, Harteveld C L, Kanavakis E, Giordano P C, Kattamis Ch, Bernini L F. Hb Aghia Sophia [α62(E11)Val→0 (α1)], an “in frame” deletion causing α-thalassemia. Hemoglobin 1999; 23(4):317–324, [PUBMED], [INFOTRIEVE], [CSA]
- Harteveld C L, Beijer C, van Delft P, Zanardini R M, Bernini L F, Giordano P C. α-Thalassaemia as a result of a novel splice donor site mutation of the α1-globin gene. Br J Haematol 2000; 110(3):694–698, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Derbally R, Mach-Pascual S, Rose K, Graf J, Beris Ph. Haemoglobin Tunis-Bizerte: a new α1 globin 129 Leu→Pro unstable variant with thalassaemic phenotype. Br J Haematol 1995; 90(1):71–76, [CSA]
- Guida V, Colosimo A, Fiorito M, Foglietta E, Bianco I, Ivalda G, Fichera M, Dallapiccola B. Denaturing HPLC-based assay for molecular screening of nondeletional mutations causing α-thalassemias. Clin Chem 2004; 50(7):1242–1245., [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Wang W, Ma E SK, Chan Q YY, Chui D HK, Chong S S. Multiple minisequencing screen for seven Southeast Asian nondeletional α-thalassemia mutations. Clin Chem 2003; 49(5):800–803, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]
- Fei Y-J, Öner R, Bozkurt G, Gu L-H, Altay Ç, Gürgey A, Fattoum S, Baysal E, Huisman T HJ. Hb H disease caused by homozygosity for the AATAAA→AATAAG mutation in the polyadenylation site of the α2-globin gene: hematological observation. Acta Heamatol 1992; 88(2–3):82–85, [CSA]
- Zorai A, Harteveld C L, Bakir A, Van Delft P, Falfoul A, Dellagi K, Abbes S, Giordano P C. Molecular spectrum of α-thalassemia in Tunisia: epidemiology and detection at birth. Hemoglobin 2002; 26(4):353–362, [PUBMED], [INFOTRIEVE], [CROSSREF], [CSA]