REFERENCES
- Huisman THJ, Carver MFH. The β- and δ-thalassemia repository (ninth edition, part I). Hemoglobin 1998; 22(2)169–195, [INFOTRIEVE], [CSA]
- Orkin SH, Kazazian HH, Jr, Antonorakis SE, Goff SC, Boehm CD, Sexton JP, Waber PG, Giardina PJV. Linkage of β thalassaemia mutations and β globin gene polymorphisms in human β globin gene cluster. Nature 1982; 296(5858)627–631, [INFOTRIEVE], [CROSSREF], [CSA]
- Antonarakis SE, Boehm CD, Giardina PJV, Kazazian HH, Jr. Non-random association of polymorphic restriction sites in the β-globin gene cluster. Proc Natl Acad Sci USA 1982; 79(1)137–141, [INFOTRIEVE], [CROSSREF], [CSA]
- Kazazian HH, Jr, Orkin SH, Markham AF, Chapman CR, Youssoufian H, Waber PG. Quantification of the close association between DNA haplotypes and specific β-thalassemia mutations in Mediterraneans. Nature 1984; 310(5973)152–154, [INFOTRIEVE], [CROSSREF], [CSA]
- Wajcman H, Krishnamoorthy R. Thalassemia in Tunisia: more tasks ahead. Hemoglobin 2004; 28(3)171–172, [CROSSREF], [CSA]
- Fattoum S, Messaoud T, Bibi A. Molecular basis of β-thalassemia in the population of Tunisia. Hemoglobin 2004; 28(3)177–187, [INFOTRIEVE], [CROSSREF], [CSA]
- Chouk I, Ben Daoud B, Mellouli F, Bejaoui M, Gerard N, Dellagi K, Abbes S. Contribution to the description of the β-thalassemia spectrum in Tunisia and the origin of mutation diversity. Hemoglobin 2004; 28(3)189–195, [INFOTRIEVE], [CROSSREF], [CSA]
- Jacquette A, Le Roux G, Lacombe C, Goossens M, Pissard S. Compound heterozygosity for two new mutations in the β-globin gene [codon 9 (+TA) and polyadenylation site (AATAAA→AAAAAA)] leads to thalassemia intermedia in a Tunisian patient. Hemoglobin 2004; 28(3)243–248, [INFOTRIEVE], [CROSSREF], [CSA]
- Fattoum S, Öner C, Li HW, Guemira F, Huisman THJ. β-Thalassemia in Tunisia: detection of some rare mutations including a newly discovered frameshift at codons 25/26 (+T). Blood 1990; 76(10 Suppl 1)60a, [CSA]
- Vidaud M, Gattoni R, Stevenin J, Vidaud D, Amselem S, Chibani J, Rosa J, Goossens M. A 5′ Slice region G→C mutation in exon 1 of the human β-globin gene inhibits pre-mRNA splicing: a mechanism for β+-thalassemia. Proc Natl Acad Sci USA 1989; 86(3)1041–1045, [INFOTRIEVE], [CROSSREF], [CSA]
- Chibani J, Vidaud M, Duquesnoy P, Bergé-Lefranc JL, Pirastu M, Ellouze F, Rosa J, Goossens M. The peculiar spectrum of β thalassemia genes in Tunisia. Hum Genet 1988; 78(2)190–192, [INFOTRIEVE], [CROSSREF], [CSA]
- Poncz M, Solowiejczyk D, Harpel B, Mory Y, Schwartz E, Surrey S. Construction of human gene libraries from small amounts of peripheral blood: analysis of β-like globin genes. Hemoglobin 1982; 6(1)27–36, [INFOTRIEVE], [CSA]
- Maggio A, Giambona A, Cai SP, Wall J, Kan YW, Chehab FF. Rapid and simultaneous typing of Hemoglobin S, hemoglobin C and seven Mediterranean β-thalassemia mutations by covalent reverse dot blot analysis: application to prenatal diagnosis in Sicily. Blood 1993; 81(1)239–242, [INFOTRIEVE], [CSA]
- Sutton M, Bouhassira EE, Nagel RL. Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes. Am J Hematol 1989; 32(1)66–69, [INFOTRIEVE], [CSA]
- Furnumi H, Firdous N, Inoue T, Ohta H, Winichagoom P, Fuchaoen S, Fukumaki Y. Molecular basis of β thalassemia in the Maldives. Hemoglobin 1998; 22(2)141–151, [CSA]
- Khan SN, Riazuddin S, Galanello R. Identification of three rare β-thalassemia mutations in the Pakistani population. Hemoglobin 2000; 24(1)15–22, [INFOTRIEVE], [CSA]
- Orkin SH, Kazazian HH, Jr. The mutation and polymorphism of the human β-globin gene and its surrounding DNA. Annu Rev Genet 1984; 18: 131–171, [INFOTRIEVE], [CROSSREF], [CSA]
- Baysal E, Huisman THJ. Detection of common deletional α-thalassemia-2 determinants by PCR. Am J Hematol 1994; 46(3)208–213, [INFOTRIEVE], [CSA]
- Abbes S, Fattoum S, Vidaud M, Goossens M, Rosa J. Sickle cell anemia in the Tunisian population: haplotypinng and Hb F expression. Hemoglobin 1991; 15(1)1–9, [INFOTRIEVE], [CSA]
- Gonzalez-Redondo JM, Stoming TA, Kutlar F, Kutlar A, Hu H, Wilson JB, Huisman THJ. Hb Monroe or α2β230(B12)Arg→Thr, a variant associated with β-thalassemia due to a G→C substitution adjacent to the donor splice site of the first intron. Hemoglobin 1989; 13(1)67–74, [INFOTRIEVE], [CSA]
- Bennani C, Tamouza R, Rouabhi F, Benabadji M, Malou M, Elion J, Labie D, Beldjord C. The spectrum of β-thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy. Br J Hematol 1993; 84(2)335–337, [CSA]
- Lie-Injo LE, Cai SP, Wahidijat I, Moeslichan S, Lim ML, Evangelista L, Doherty M, Kan YW. β‐Thalassemia mutations in Indonesia and their linkage to β haplotypes. Am J Hum Genet 1989; 45(6)971–975, [INFOTRIEVE], [CSA]
- El-Kalla S, Mathews AR. A significant β-thalassemia heterogeneity in the United Arab Emirates. Hemoglobin 1997; 21(3)237–247, [INFOTRIEVE], [CSA]
- Yavarian M, Harteveld CL, Batelaan D, Bernini LF, Giordano PC. Molecular spectrum of β-thalassemia in the Iranian province of Hormozgan. Hemoglobin 2001; 25(1)35–43, [INFOTRIEVE], [CROSSREF], [CSA]
- Gorakshakar AC, Lulla CP, Nadkarni AH, Pawar AR, Desai SN, Colah RB, Mohanty D. Prenatal diagnosis of β-thalassemia among Indians using denaturing gradient gel electrophoresis. Hemoglobin 1994; 21(5)421–435, [CSA]
- Old JM, Khan SN, Verma I, Fucharoen S, Kleanthous M, Ioannou P, Kotea N, Fisher C, Riazuddin S, Saxena R, Winichagoon P, Kyriacou K, Al-Quobaili F, Khan B. A multi-center study in order to further define the molecular basis of β-thalassemia in Thailand, Pakistan, Sri Lanka, Mauritius, Syria, and India, and to develop a simple molecular diagnostic strategy by amplification refractory mutation system-polymerase chain reaction. Hemoglobin 2001; 25(4)397–407, [INFOTRIEVE], [CROSSREF], [CSA]
- Dedoussis G, Mandilara G, Boussiu M, Loutradis A. Hb F production in β-thalassemia heterozygotes for the IVS-II-1 G→A β0-globin mutation. Implication of the haplotype and the Gγ −158 C→T mutation on the Hb F level. Am J Hematol 2000; 64(3)151–155, [INFOTRIEVE], [CROSSREF], [CSA]
- Bouhass R, Perrin P, Trabuchet G. The spectrum of β-thalassemia mutations in the Oran region of Algeria. Hemoglobin 1994; 18(3)211–219, [INFOTRIEVE], [CSA]
- Gonzalez-Redondo JM, Stoming TA, Kutlar F, Kutlar A, McKie KM, Huisman THJ. Severe Hb S-β0-thalassaemia with a T→C substitution in the donor splice site of the first intron of the β-globin gene. Br J Hematol 1989; 71(1)113–117, [CSA]
- Bouhass R, Aguercif M, Trabuchet G, Godet J. A new mutation at IVS-I nt 2 (T→A) in β-thalassemia from Algeria. Blood 1990; 76(5)1054–1055, [INFOTRIEVE], [CSA]