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Hemoglobin
international journal for hemoglobin research
Volume 13, 1989 - Issue 1
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Original Article

High Frequencies of a Rearrangement (+ATA; -T) at -530 to the β-Globin Gene in Different Populations Indicate the Absence of a Correlation with a Silent β-Thalassemia Determinant

S. C. Wong Department of Cell, Molecular Biology Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
T. A. Stoming Department of Cell, Molecular Biology Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
G. D. Efremov Macedonian Academy of Sciences and Arts Research Center for New Technologies, 91000, Skopje, Yugoslavia
&
T. H. J. Huisman Department of Cell, Molecular Biology Medical College of Georgia, Augusta, GA, 30912-2100, USA
Pages 1-5 | Received 28 Jun 1988, Accepted 16 Aug 1988, Published online: 07 Jul 2009

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D. Labie & J. Elion. (1996) Sequence Polymorphisms of Potential Functional Relevance in the β-Globin Gene Locus. Hemoglobin 20:2, pages 85-101.
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G. Zhou, M-J. Chen, Z-R. Ren, S-Z. Huang & Y-T. Zeng. (1995) Patternf the (At)XTY Motif At The -530 Region 5′ To The β-Globin Gene In The Chinese Population. Hemoglobin 19:5, pages 311-316.
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R. B. Gupta, R. S. Tiwary, P. L. Pande, F. Kutlar, C. Öner, R. Öner & T. H. J. Huisman. (1991) Hemoglobinopathies Among the Gond Tribal Groups of Central India; Interaction of α- and β-Thalassemia with β Chain Variants. Hemoglobin 15:5, pages 441-458.
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Articles from other publishers (17)

Latifa Jouini, Amina Bibi, Faida Ouali, Sondess Hadj Fredj, Fekria Ouennich, Hajer Siala, Taieb Messaoud & Slaheddine Fattoum. (2011) Contribution of β-globin cluster polymorphisms to raise fetal hemoglobin levels in normal adults. Molecular Biology Reports 39:4, pages 4619-4625.
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Sanmay Bandyopadhyay, Bama Charan Mondal, Pabak Sarkar, Sarmila Chandra, M. K. Das & Uma B. Dasgupta. (2005) Two beta-globin cluster-linked polymorphic loci in thalassemia patients of variable levels of fetal hemoglobin. European Journal of Haematology 75:1, pages 47-53.
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Jun Ohashi, Izumi Naka, Jintana Patarapotikul, Hathairad Hananantachai, Gary Brittenham, Sornchai Looareesuwan, Andrew G. Clark & Katsushi Tokunaga. (2004) Strong linkage disequilibrium of a HbE variant with the (AT)9(T)5 repeat in the BP1 binding site upstream of the β-globin gene in the Thai population. Journal of Human Genetics 50:1, pages 7-11.
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Antonio Cao & Paolo Moi. (2002) Regulation of the Globin Genes. Pediatric Research 51:4, pages 415-421.
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Vassiliki Kalotychou, Panagoula Kollia, Ersi Voskaridou, Theoharis Patargias, Nicholas P. Anagnou & Dimitris Loukopoulos. (2002) Functional Role of the Four Different Types of (AT)XTY Motifs 5′ to the β-Globin Gene and Their Distribution in the Greek Population. Blood Cells, Molecules, and Diseases 28:1, pages 39-46.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Antonio Cao & Paolo Moi. (2000) Genetic Modifying Factors in β-Thalassemia. cclm 38:2, pages 123-132.
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Swee Lay Thein. (1998) 3 β-Thalassaemia. Baillière's Clinical Haematology 11:1, pages 91-126.
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Pranee Winichagoon, Suthat Fucharoen, Prapon Wilairat, Kazuo Chihara & Yasuyuki Fukumaki. (2008) Nondeletional type of hereditary persistence of fetal haemoglobin: molecular characterization of three unrelated Thai HPFH. British Journal of Haematology 87:4, pages 797-804.
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A. J. Dimovski, A. D. Adekile, V. Divoky, E. Baysal & T. H. J. Huisman. (2006) Polymorphic pattern of the (AT) x (T) y motif at −530 5′ to the β‐globin gene in over 40 patients homozygous for various β‐thalassemia mutations . American Journal of Hematology 45:1, pages 51-57.
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Swee Lay Thein. (1993) 6 β-Thalassaemia. Baillière's Clinical Haematology 6:1, pages 151-175.
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G. W. Hall, R. A. Barnetson & S. L. Thein. (2008) Beta thalassaemia in the indigenous British population. British Journal of Haematology 82:3, pages 584-588.
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S. Murru, G. Loudianos, S. Porcu, G. V. Sciarratta, S. Agosti, M. I. Parodi, A. Cao & M. Pirastu. (2008) A β‐thalassaemia phenotype not linked to the β‐globin cluster in an Italian family. British Journal of Haematology 81:2, pages 283-287.
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Cihan �ner, AleksandarJ. Dimovski, NancyF. Olivieri, Gino Schiliro, JohnF. Codrington, Sladdehine Fattoum, AdekunleD. Adekile, Reyhan �ner, GunesT. Y�regir, C. Altay, A. Gurgey, RashikB. Gupta, VinodB. Jogessar, MichaelN. Kitundu, Dimitris Loukopoulos, GabrielP. Tamagnini, M.LeticiaS. Ribeiro, Ferdane Kutlar, Li-Hao Gu, KennethD. Lanclos & TitusH.J. Huisman. (1992) ?s Haplotypes in various world populations. Human Genetics 89:1, pages 99-104.
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S. Murru, D. Poddie, G. V. Sciarratta, S. Agosti, M. Baffico, C. Melevendi, M. Pirastu & A. Cao. (1992) A novel β-globin structural mutant, Hb Brescia (β114 Leu-Pro), causing a severe β-thalassemia intermedia phenotype. Human Mutation 1:2, pages 124-128.
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Patricia E. Berg, Moshe Mittelman, Jacques Elion, Dominique Labie & Alan N. Schechter. (2006) Increased protein binding to a −530 mutation of the human β‐globin gene associated with decreased β‐globin synthesis. American Journal of Hematology 36:1, pages 42-47.
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M. PIRASTU, M. S. RISTALDI, G. LOUDIANOS, S. MURRU, G. V. SCIARRATTA, M. I. PARODI, D. LEONE, S. AGOSTI & A. CAO. (1990) Molecular Analysis of Atypical ?-Thalassemia Heterozygotes. Annals of the New York Academy of Sciences 612:1 Sixth Cooley', pages 90-97.
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