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• W4205981346 abstract "Free Access References D.J. Weatherall, D.J. WeatherallSearch for more papers by this authorJ.B. Clegg, J.B. CleggSearch for more papers by this author Book Author(s):D.J. Weatherall, D.J. WeatherallSearch for more papers by this authorJ.B. Clegg, J.B. CleggSearch for more papers by this author First published: 01 January 2001 https://doi.org/10.1002/9780470696705.refs AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature References Aasland, R., Gibson, T.J. & Stewart, A.F. (1995) The PHD finger: implications for chromatin-mediated transcriptional regulation. Trends Biol. Sci. 20, 56. CrossrefCASPubMedWeb of Science®Google Scholar Abbondanzo, S.L., Anagnou, N.P. & Sacher, R.A. (1988) Myelodys-plastic syndrome with acquired hemoglobin H disease. Am. J. Clin. Pathol. 89, 401. CrossrefCASPubMedWeb of Science®Google Scholar Abdalla, S.H., Corrah, P.T. & Higgs, D.R. (1989) α-Thalassaemia in The Gambia. Trans. Roy. Soc. Trop. Med. Hyg. 83, 420. CrossrefCASPubMedWeb of Science®Google Scholar Abels, J., Michiels, J.J., Giordano, P.C. et al. (1996) A de novo deletion causing εγδβ-thalassemia in a Dutch patient. Acta Haematol. 96, 108. CrossrefCASPubMedWeb of Science®Google Scholar Abraham, E.C., Walker, D., Gravely, M. & Huisman, T.H.J. (1975) Minor hemoglobins in sickle cell anemia, β-thalassemia: a study of red cell fractions isolated by density gradient centrifugation. Biochem. Med. 11, 56. CrossrefWeb of Science®Google Scholar Abramson, R.K., Rucknagel, D.L., Shreffler, D.C. & Saave, J.J. (1970) Homozygous Hb J Tongariki: evidence for only one alpha chain structural locus in Melanesians. Science 169, 194. CrossrefCASPubMedWeb of Science®Google Scholar Abreu de Miani, M.S. & Peñalver, J.A. (1983) Incidencia de porta-dores beta-talasémicos y de deficientes de la glucosa-6-fosfato dehidrogenasa eritrocítica (G6PD) en el área del Gran Buenos Aires. Sangre, 28, 537. CASPubMedGoogle Scholar Abuelo, D.N., Forman, E.N. & Rubin, L.P. (1997) Limb defects and congenital anomalies of the genitalia in an infant with homozygous α-thalassemia. Am. J. Med. Genet. 68, 158. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Abu-Sin, A., Felice, A.E., Gravely, M.E. et al. (1979) Hb P-Nilotic in association with β-thalassemia: cis-mutation of a hemoglobin βA chain regulatory determinant. J. Lab. Clin. Med. 93, 973. CASPubMedWeb of Science®Google Scholar Acquaye, C.T.A., Oldham, J.H. & Konotey-Ahulu, F.I.D. (1977) Blood donor homozygous for hereditary persistence of fetal haemoglobin. Lancet i, 796. CrossrefGoogle Scholar Adachi, K., Surrey, S., Temery, H. et al. (1993) Hb Shelby [beta131 (H9)Gln→Lys] in association with Hb S [beta 6(A3)Glu→Val]: characterization, stability and effects on Hb S polymerization. Hemoglobin 17, 329. CrossrefCASPubMedWeb of Science®Google Scholar Adamkiewicz, T.V., Berkovitch, M., Krishnan, C., Polsinelli, K., Kermack, D. & Olivieri, N.F. (1998) Yersinia enterocolitica and beta thalassemia: a report of 15 years' experience. Clin. Infect. Dis. 27, 1367. PubMedWeb of Science®Google Scholar Adams, W.H. (1974) A survey for haemoglobinopathies in Nepal. Trans. Roy. Soc. Trop. Med. Hyg. 68, 392. CrossrefCASPubMedWeb of Science®Google Scholar M.B. Adams (ed.), (1990) The Wellborn Science: Eugenics in Germany, France, Brazil and Russia. Oxford University Press, Oxford. Google Scholar Adams, J. G. III & Coleman, M.B. (1990) Structural hemoglobin vari-ants that produce the phenotype of thalassemia. Sem. Hematol. 27, 229. CASPubMedWeb of Science®Google Scholar Adams, J.G. III, Steinberg, M.H., Newman, M.V., Morrison, W.T., Benz, E.J. & Iyer, R. (1981) β-Thalassemia present in cis to a new β-chain structural variant, Hb Vicksburg [β75(E19)Leu→O]. Proc. Natl Acad. Sci. USA 78, 469. CrossrefCASPubMedWeb of Science®Google Scholar Adams, J.G. III, Morrison, W.T. & Steinberg, M.H. (1982) Double crossover within a human gene. Science 218, 241. CrossrefPubMedWeb of Science®Google Scholar Adams, J.G. III, Coleman, M.B., Hayes, J., Morrison, W.T. & Steinberg, M.H. (1985) Modulation of fetal hemoglobin synthesis by iron deficiency. N. Eng. J. Med. 313, 1402. CrossrefPubMedWeb of Science®Google Scholar Adams, J.G. III, Steinberg, M.H. & Kazazian, H.H.J. (1990) Isolation and characterization of the translation product of a β-globin gene nonsense mutation (β121GAA→TAA). Br. J. Haematol. 75, 561. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Adams, R.J., Kutlar, A., McKie, V. et al. (1994) Alpha thalassemia and stroke risk in sickle cell anemia. Am. J. Hematol. 45, 279. Wiley Online LibraryPubMedWeb of Science®Google Scholar Adams, R.J., McKie, V.C., Hsu, L. et al. (1998) Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography. N. Eng. J. Med. 333, 5. CrossrefWeb of Science®Google Scholar Adamson, J.W. (1975) Familial polycythemia. Sem. Hematol. 12, 383. PubMedWeb of Science®Google Scholar Adekile, A.D. (1997) Historical and anthropological correlates of βS haplotypes and α- and β-thalassemia alleles in the Arabian Peninsula. Hemoglobin 21, 281. CrossrefCASPubMedWeb of Science®Google Scholar Adekile, A.D. & Haider, M.Z. (1996) Morbidity, βS haplotype and α-globin gene patterns among sickle cell anemia patients in Kuwait. Acta Haematol. 96, 150. CrossrefCASPubMedWeb of Science®Google Scholar Advani, R., Rubin, E., Mohandas, N. & Schrier, S.L. (1992a) Oxidative red blood cell membrane injury in the pathophysiology of severe mouse beta-thalassemia. Blood 79, 1064. CASPubMedWeb of Science®Google Scholar Advani, R., Sorenson, S., Shinar, E., Lande, W., Rachmilewitz, E. & Schrier, S.L. (1992b) Characterization and comparison of the red blood cell membrane damage in severe human alpha- and beta-thalassemia. Blood 79, 1058. CASPubMedWeb of Science®Google Scholar Advisory Committee on Genetic Testing, (1997) Code of Practice and Guidance on Human Genetic Testing Services Supplied Direct to the Public. Department of Health, London. Google Scholar Aessopos, A., Voskaridou, E., Kavouklis, E. et al. (1994) Angioid streaks in sickle-thalassemia. Am. J. Ophthalmol. 117, 589. CrossrefPubMedWeb of Science®Google Scholar Aessopos, A., Stamatelos, G., Skoumas, V., Vassilopoulos, G., Mantzourani, M. & Loukopoulos, D. (1995) Pulmonary hyperten-sion and right heart failure in patients with β-thalassemia inter-media. Chest 107, 50. CrossrefPubMedWeb of Science®Google Scholar Afifi, A.M. (1974) High transfusion regime in the management of reproductive wastage and maternal complications of pregnancy in thalassaemia major. Acta Haematol. 52, 331. CrossrefCASPubMedWeb of Science®Google Scholar Agarwal, M.B., Viswanathan, C., Ramananthan, J. et al. (1990) Oral iron chelation with L1. Lancet 335, 601. CrossrefCASPubMedWeb of Science®Google Scholar Agarwal, M.B., Gupte, S.S., Viswanathan, C et al. (1992) Long-term assessment of efficacy and safety of L1, an oral iron chelator, in transfusion-dependent thalassaemia: Indian trial. Br. J. Haematol. 82, 460. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Agarwal, S., Gulati, R. & Singh, K. (1997) Hemoglobin E-beta thalassemia in Uttar Pradesh. Indian Ped. 34, 287. CASPubMedGoogle Scholar Ager, J.A.M. & Lehmann, H. (1958) Observations on some ‘fast’ haemoglobins: K., J., N and Bart's. Br. Med. J. i, 929. CrossrefCASWeb of Science®Google Scholar Ahern, E.J., Ahern, V.N., Jones, R.T. & Brimhall, B. (1972) Hemoglo-bin Lepore Washington in two Jamaican families: interaction with beta chain variants. Blood 40, 246. CASPubMedWeb of Science®Google Scholar Ahern, E., Herbert, R., McIver, C., Ahern, V., Wardle, J. & Seakins, M. (1975) Beta-thalassaemia of clinical significance in adult Jamaican Negroes. Br. J. Haematol. 30, 197. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Ahmed, S., Petrou, M. & Saleem, M. (1996) Molecular genetics of β-thalassaemia in Pakistan: a basis for prenatal diagnosis. Br. J. Haematol. 94, 476. CASPubMedWeb of Science®Google Scholar Ajmani, M., Sharma, A., Talukder, G. & Bhattacharya, D.K. (1976) Beta-thalassaemia trait in West Bengal —a methodological study. Curr. Sci. 45, 461. CASWeb of Science®Google Scholar Aksoy, M. (1959) Abnormal haemoglobins in Turkey. In: Abnormal Haemoglobins—A Symposium (eds J. H. P. Jonxis & J. F. Delafres-naye), p. 216. Blackwell Scientific Publications, Oxford. Google Scholar Aksoy, M. (1963) The first observation of homozygous hemoglobin S-alpha thalassemia disease and two types of sickle cell disease: (a) sickle cell-alpha thalassemia disease (b) sickle cell-beta thalassemia disease. Blood 22, 757. CASPubMedWeb of Science®Google Scholar Aksoy, M. (1970) Thalassaemia intermedia: a genetic study in 11 patients. J. Med. Genet. 7, 47. CrossrefCASPubMedGoogle Scholar Aksoy, M. (1991) The history of beta-thalassemia in Turkey. Turkish J. Pediatr. 33, 195. CASWeb of Science®Google Scholar Aksoy, M. & Erdem, S. (1968a) Combination of hereditary elliptocy-tosis and heterozygous beta-thalassaemia: a family study. J. Med. Genet. 5, 298. CrossrefCASPubMedGoogle Scholar Aksoy, M. & Erdem, S. (1968b) The combination of hereditary sphe-rocytosis and heterozygous beta-thalassaemia. A family study. Acta Haematol. (Basel) 39, 183. CrossrefCASPubMedWeb of Science®Google Scholar Aksoy, M. & Erdem, S. (1968c) Haemoglobin H disease. Study of an Eti-Turk family. Acta Genet. 18, 12. CASPubMedWeb of Science®Google Scholar Aksoy, M. & Lehmann, H. (1957) Sickle-cell-thalassaemia disease in South Turkey. Br. Med. J. i, 734. CrossrefWeb of Science®Google Scholar Aksoy, M., Egribozlu, A. & Alpustun, H. (1961) The thalassaemia syndromes. I. Thalassaemia minor with large amount of foetal haemoglobin. Study of a family. Acta Haematol. 25, 136. CrossrefCASPubMedWeb of Science®Google Scholar Aksoy, M., Cetingil, A.I., Kocabalkan, N. et al. (1963) Thalassemia-hemoglobin E disease in Turkey, with hypersplenism in one case. Am. J. Med. 34, 851. CrossrefCASPubMedWeb of Science®Google Scholar Aksoy, M., Camili, N., Dincol, K., Erdem, S. & Dincol, G. (1973) On the problem of ‘rib-within-a-rib’ appearance in thalassemia inter-media. Radiol. Clin. Biol. 42, 126. CASPubMedWeb of Science®Google Scholar Aksoy, M., Erdem, S. & Dincol, G. (1974) Delta beta-thalassaemia in two Turkish families. J. Med. Genet. 11, 337. CrossrefCASPubMedWeb of Science®Google Scholar Aksoy, M., Erdem, S. & Dincol, G. (1975) β-Thalassemia with normal levels of hemoglobins F and A2. Simple heterozygous and homozygous forms and doubly heterozygous state with β-thalassemia with increased hemoglobin A2. Study in seven families. In: Proceedings of the International Instanbul Symposium on Abnormal Hemoglobins and Thalassemia, p. 289. TBTAK, Ankara. Google Scholar Aksoy, M., Dincol, G. & Erdem, S. (1978a) Different types of beta-thalassaemia intermedia. Acta Haematol. (Basel) 59, 178. CrossrefCASPubMedWeb of Science®Google Scholar Aksoy, M., Tahsinoglu, M., Erdem, S. & Dincol, G. (1978b) Myelofi-brosis in a case of Hb E-β+ thalassemia. New Istanbul Contrib. Clin. Sci. 12, 279. CASPubMedGoogle Scholar Aksoy, M., Kutlar, A., Kutlar, F. et al. (1984) Hb Beograd-β0 thalassemia in a Turkish family from Yugoslavia. Hemoglobin 8, 417. CrossrefCASPubMedWeb of Science®Google Scholar Aksoy, M., Kutlar, A., Kutlar, F., Dinçol, G., Erdem, S. & Bastesbihçi, S. (1985) Survey on haemoglobin variants, β thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglo-bin types in Turks from Western Thrace. J. Med. Genet. 22, 288. CrossrefCASPubMedWeb of Science®Google Scholar Alam, R., Padmanabhan, K. & Rao, H. (1997) Paravertebral mass in a patient with thalassemia intermedia. Chest 112, 265. CrossrefCASPubMedWeb of Science®Google Scholar Alberti, R., Maruzzi, G.M., Marinucci, M., Bruni, E. & Tentori, L. (1975) Haemoglobin Hasharon in a north Italian community. J. Med. Genet. 12, 294. CrossrefCASPubMedWeb of Science®Google Scholar Alberti, R., Tentori, L., Martinucci, M. & Borghesi, V. (1978) Hb A2-Adria (δ51 Pro yield Arg (D2): a new δ-chain variant found in association with β-thalassemia. Hemoglobin 2, 171. CrossrefCASPubMedWeb of Science®Google Scholar Alberts, B., Bray, D., Lewis, J., Raff, M., Roberts, K. & Watson, J.B. (1994) The Molecular Biology of the Cell. Garland, New York and London. Google Scholar Albitar, M., Peschle, C. & Liebhaber, S.A. (1989) Theta, zeta and epsilon globin messenger RNAs are expressed in adults. Blood 74, 629. CASPubMedWeb of Science®Google Scholar Albitar, M., Katsumata, M. & Liebhaber, S.A. (1991) Human α-globin genes demonstrate autonomous developmental regulation in transgenic mice. Mol. Cell. Biol. 11, 3786. CrossrefCASPubMedWeb of Science®Google Scholar Aldouri, M.A., Wonke, B., Hoffbrand, A.V. et al. (1987) Iron state and hepatic disease in patients with thalassaemia major treated with long term subcutaneous desferrioxamine. J. Clin. Pathol. 40, 1352. CrossrefWeb of Science®Google Scholar Aldouri, M.A., Wonke, B., Hoffbrand, A.V. et al. (1990) High inci-dence of cardiomyopathy in beta-thalassaemia patients receiving regular transfusion and iron chelation: reversal by intensified chelation. Acta Haematol. 84, 113. CrossrefPubMedWeb of Science®Google Scholar Ali, M.A.M. & McBride, J.A. (1973) Globin synthesis in haemoglo-bin Lepore trait. Br. J. Haematol. 25, 284. CASPubMedWeb of Science®Google Scholar Ali, M.A.M., Quinlan, A. & Wong, S.C. (1980) Identification of hemoglobin E by isopropanol solubility test. Clin. Biochem. 13, 146. CrossrefCASPubMedWeb of Science®Google Scholar Aljurf, M., Ma, L., Angelucci, E. et al. (1996) Abnormal assembly of membrane proteins in erythroid progenitors of patients with beta-thalassemia major. Blood 87, 2049. CASPubMedWeb of Science®Google Scholar Al-Khatti, A., Veith, R.A., Papayannopoulou, T., Fritsch, E.F., Goldwasser, E. & Stamatoyannopoulos, G. (1987) Stimulation of fetal hemoglobin synthesis by erythropoietin in baboons. N. Eng. J. Med. 317, 415. CrossrefCASPubMedWeb of Science®Google Scholar Allamanis, J. (1955) Paper electrophoresis of serum proteins in Cooley's anaemia and sickle cell anaemia. Acta Paediatr. 44, 122. Wiley Online LibraryCASPubMedGoogle Scholar Allen, S.J., O'Donnell, A., Alexander, N.D.E. et al. (1997) a+-Thalassaemia protects children against disease caused by other infections as well as malaria. Proc. Natl Acad. Sci. USA 94, 14736. CrossrefCASPubMedWeb of Science®Google Scholar Allison, A.C. (1954) Protection afforded by sickle-cell trait against subtertian malarial infection. Br. Med. J. i, 290. CrossrefCASWeb of Science®Google Scholar Allison, A.C. (1964) Polymorphism and natural selection in human populations. Cold Spring Harbor Sympos. Quant. Biol. 29, 137. CrossrefCASPubMedWeb of Science®Google Scholar Allison, A.C. (1965) Population genetics of abnormal haemoglobins and glucose-6-phosphate dehydrogenase deficiency. In: Abnor-mal Haemoglobins in Africa (ed. J. H. P. Jonxis), p. 365. Blackwell Scientific Publications, Oxford. Google Scholar Aloia, J.F., Ostuni, J.A., Yeh, J.K. & Zaino, E.C. (1982) Combined vit-amin D parathyroid defect in thalassemia major. Arch. Intern. Med. 142, 831. CASPubMedWeb of Science®Google Scholar Al-Refaie, F.N., Wonke, B., Hoffbrand, A.V., Wickens, D.G., Nortey, P. & Kontoghiorghes, G.J. (1992) Efficacy and possible adverse effects of the oral iron chelator 1, 2-dimethyl-3-hydroxypyrid-4-one (L1) in thalassemia major. Blood 80, 592. Google Scholar Al-Refaie, F.N., Hershko, C., Hoffbrand, A.V. et al. (1995) Results of long-term deferiprone (L1) therapy. A report by the International Study Group on Oral Iron Chelators. Br. J. Haematol. 91, 224. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Altay, C., Huisman, T.H.J. & Schroeder, W.A. (1976–77) Another form of hereditary persistence of fetal hemoglobin (the Atlanta type)? Hemoglobin 1, 125. CrossrefCASPubMedWeb of Science®Google Scholar Altay, C., Say, B., Yetgin, S. & Huisman, T.H.J. (1977a) α-Thalassemia and β-thalassemia in a Turkish family. Am. J. Hematol. 2, 1. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Altay, C., Schroeder, W.A. & Huisman, T.H.J. (1977b) The Gγ-δβ-thalassemia and Gγ-β0-HPFH conditions in combination with β-thalassemia and Hb S. Am. J. Hematol. 3, 1. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Altay, C., Kutlar, A., Wilson, J.B., Webber, B.B. & Huisman, T.H.J. (1987) Hb P-Nilotic or 2(βδ)2 in a Turkish family. Hemoglobin 11, 395. CrossrefCASPubMedWeb of Science®Google Scholar Altay, C., Gurgey, A., Öner, R., Kutlar, A., Kutlar, F. & Huisman, T.H.J. (1991) A mild thalassemia major resulting from a com-pound heterozygosity for the IVS-II-1 (G-A) mutation and the rare T-C mutation at the polyadenylation site. Hemoglobin 15, 327. CrossrefCASPubMedWeb of Science®Google Scholar Alter, B.P. (1979) The Gγ:Aγ composition of fetal hemoglobin in fetuses and newborns. Blood 54, 1158. CASPubMedWeb of Science®Google Scholar Alter, B.P. (1984) Advances in the prenatal diagnosis of hematologic diseases. Blood 64, 329. CrossrefCASPubMedWeb of Science®Google Scholar Alter, B.P. (1989) Examination of fetal blood for haemoglo-binopathies. In: Methods in Haematology: Perinatal Haematology (ed. B.P. Alter), p. 13. Churchill Livingstone, Edinburgh. Google Scholar Alter, B.P. (1990) Antenatal diagnosis. Summary of results. Ann. N. Y. Acad. Sci. 612, 237. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Alter, B.P. & Nathan, D.G. (1978) Antenatal diagnosis of haemato-logical disorders —1978. Clin. Haematol. 7, 19. PubMedWeb of Science®Google Scholar Alter, B.P, Friedman, S., Hobbins, J.C. et al. (1976a) Prenatal diagnosis of sickle-cell anemia and alpha G-Philadelphia. Study of a fetus at risk for Hb S/β thalassemia. N. Eng. J. Med. 294, 1040. CrossrefCASPubMedWeb of Science®Google Scholar Alter, B.P., Modell, C.B., Fairweather, D. et al. (1976b) Prenatal diagnosis of hemoglobinopathies. A review of 15 cases. N. Eng. J. Med. 295, 1437. CrossrefCASPubMedWeb of Science®Google Scholar Alter, B.P, Rappeport, J.M., Huisman, T.H.J., Schroeder, W.A. & Nathan, D.G. (1976c) Fetal erythropoiesis following bone marrow transplantation. Blood 48, 843. PubMedWeb of Science®Google Scholar Alter, B.P, Metzger, J.B., Yock, P.G., Rothchild, S.B. & Dover, G.J. (1979a) Selective hemolysis of adult red blood cells: an aid to prenatal diagnosis of hemoglobinopathies. Blood 53, 279. CASPubMedWeb of Science®Google Scholar Alter, B.P, Orkin, S.H. & Nathan, D.G. (1979b) Prenatal diagnosis of the hemoglobinopathies. In: Laboratory Investigation of Fetal Disease (ed. A. J. Barson), p. 337. Wright and Sons Ltd, London. Google Scholar Alter, B.P, Goff, S.C., Efremov, G.D., Gravely, M.E. & Huisman, T.H.J. (1980) Globin chain electrophoresis: a new approach to the determination of the Gγ/Aγ ratio in fetal haemoglobin and to studies of globin synthesis. Br. J. Haematol. 44, 527. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Amegnizin, K.P.E., Pagnier, J., Wajcman, H., Lapoumeroulie, C. & Labie, D. (1979) Hb J Lome β59 (E3) Lys→Asn associated with HPFH in a Togolese family. Hemoglobin 3, 87. CrossrefCASPubMedWeb of Science®Google Scholar Ameri, M.R., Aleboiuyeh, M., Ziai, M. & Conn, R.B. (1975) Hyper-triglyceridemia in homozygous beta thalassemia. J. Pediatr. 87, 1002. CrossrefCASPubMedWeb of Science®Google Scholar American Association for the Advancement of Science, (1992) The Genome, Ethics and the Law: Issues in Genetic Testing. AAAS, Washington DC. Google Scholar Amin, A.B., Pandya, N.L., Diwin, P.P. et al. (1979) A comparison of the homozygous states for Gγ and GγAγ δβ thalassaemia. Br. J. Haematol. 43, 537. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Amselem, S., Nunes, V., Vidaud, M. et al. (1988) Determination of the spectrum of β-thalassemia genes in Spain by use of dot-blot analy-sis of amplified β-globin DNA. Am. J. Hum. Genet. 43, 95. CASPubMedWeb of Science®Google Scholar Anagnou, N.P, Ley, T.J., Chesbro, B. et al. (1983) Acquired α-thalassemia in preleukemia is due to decreased expression of all four α-globin genes. Proc. Natl Acad. Sci. USA 80, 6051. CrossrefCASPubMedWeb of Science®Google Scholar Anagnou, N.P, Papayannopoulou, T., Stamatoyannopoulos, G. & Nienhuis, A.W. (1985) Structurally diverse molecular deletions in the β-globin gene cluster exhibit an identical phenotype on inter-action with the βS-gene. Blood 65, 1254. Google Scholar Anagnou, N.P., Papayannopoulou, T., Nienhuis, A.W. & Stamatoyannopoulos, G. (1988) Molecular characterization of a novel form of (Aγδβ)0-thalassemia deletion with a 3′ breakpoint close to those of HPFH-3 and HPFH-4: insights for a common regulatory mechanism. Nucl. Acids Res. 16, 6057. CrossrefCASPubMedWeb of Science®Google Scholar Anagnou, N.P., Perez-Stable, C., Gelinas, R. et al. (1995) Sequences located 3′ to the breakpoint of the hereditary persistence of fetal hemoglobin-3 deletion exhibit enhancer activity and can modify the developmental expression of the human fetal Aγ-globin gene in transgenic mice. J. Biol. Chem. 270, 10256. CrossrefCASPubMedWeb of Science®Google Scholar Anapliotou, M.L., Kastanias, I.T., Psara, P., Evangelou, E.A., Liparaki, M. & Dimitriou, P. (1995) The contribution of hy-pogonadism to the development of osteoporosis in thalas-saemia major: new therapeutic approaches. Clin. Endocrinol. 42, 279. Wiley Online LibraryPubMedWeb of Science®Google Scholar Anderson, W.F. & Fletcher, J.C. (1980) Gene therapy in human beings: when is it ethical to begin. N. Eng. J. Med. 303, 1293. CrossrefCASPubMedWeb of Science®Google Scholar Anderson, B.B., Mollin, D.L., Modell, C.B. & Perry, G.M. (1975) Red-cell metabolism of pyridoxine in sideroblastic anaemia and thalassaemia. In: Iron Metabolism and Its Disorders (ed. H.E.A. Kief), p. 241. Excerpta Medica, Amsterdam. Google Scholar Anderson, B.B., Perry, G.M., Modell, C.B., Child, J.A. & Mollin, D.L. (1979) Abnormal red cell metabolism of pyridoxine associated with β-thalassaemia. Br. J. Haematol. 41, 497. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Anderson, K.P., Lloyd, J.A., Ponce, E., Crable, S.C., Neumann, J.C. & Lingrel, J.B. (1993) Regulated expression of the human β globin gene in transgenic mice requires an upstream globin or nonglobin promoter. Mol. Cell. Biol. 4, 1077. CrossrefCASPubMedWeb of Science®Google Scholar Andre, R., Najman, A., Duhamel, G. et al. (1972) Erythro-leucémie avec hémoglobine H acquise et anomalies des antigènes erythro-cytaires. Nouv. Rev. Fr. Hematol. 12, 29. CASPubMedWeb of Science®Google Scholar Andre, M., Bergmann, P., Ferster, A., Toppet, M. & Fondu, P. (1991) Serum immunoreactive erythropoietin level: a new parameter for monitoring transfusion management of thalassaemia. Nouv. Rev. Fr. Hematol. 33, 299. CASPubMedWeb of Science®Google Scholar Andreani, M., Manna, M., Lucarelli, G. et al. (1996) Persistence of mixed chimerism in patients transplanted for the treatment of thalassemia. Blood 87, 3494. CASPubMedWeb of Science®Google Scholar Andrews, N.C., Erdjument-Bromage, H., Davidson, M.B., Tempst, P. & Orkin, S.H. (1993a) Erythroid transcription factor NF/E2 is a haematopoietic-specific basic-leucine zipper protein. Nature 362, 722. CrossrefCASPubMedWeb of Science®Google Scholar Andrews, N.C., Kotkow, K.J., Ney, P.A., Erdjument-Bromage, H., Tempst, P. & Orkin, S.H. (1993b) The ubiquitous subunit of erythroid transcription factor NF-E2 is a small basic-leucine zipper protein related to the v-maf oncogene. Proc. Natl Acad. Sci. USA 90, 11488. CrossrefCASPubMedWeb of Science®Google Scholar Angastiniotis, M.A. & Hadjiminas, M.G. (1981) Prevention of thalas-saemia in Cyprus. Lancet 1, 369. CrossrefCASPubMedWeb of Science®Google Scholar Angastiniotis, M. & Modell, B. (1998) Global epidemiology of hemo-globin disorders. Ann. N. Y. Acad. Sci. 850, 251. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Angelini, V. (1937) Primi risultati di richerche ematologiche nei familiari di ammalati di anemia di Cooley. Min. Med. 28, 331. Google Scholar Angelucci, E., Baronciani, D., Lucarelli, G. et al. (1993) Liver iron overload and liver fibrosis in thalassemia. Bone Marrow Transplant. 1, 29. Google Scholar Angelucci, E., Baronciani, D., Lucarelli, G. et al. (1995) Needle liver biopsy in thalassaemia: analyses of diagnostic accuracy and safety in 1184 consecutive biopsies. Br. J. Haematol. 89, 757. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Angelucci, E., Ripalti, M., Baronciani, D. et al. (1997) Phlebotomy to reduce iron overload in patients cured of thalassemia by marrow transplantation. Bone Marrow Transplant. 19 (Suppl. 2), 123. Google Scholar Angelucci, E., Brittenham, G.M., Mclaren, C.E. et al. (2000) Hepatic iron concentration and total body iron stores in thalassaemia major. N. Eng. J. Med. 343, 327. CrossrefCASPubMedWeb of Science®Google Scholar Angles-Cano, E., Robles-Arrendondo, I., Ferrer, V., Gonzalez-Constandse, R. & Ortiz-Trejo, J.F. (1977) Talasemia alfa (hemo-globinopatía H) en una familia mestiza mexicana. Sangre 22, 366. CASPubMedWeb of Science®Google Scholar Anneren, G. & Gustavson, K.-H. (1984) Partial trisomy 3q (3q25→qter) syndrome in two siblings. Acta Paediatr. Scand. 73, 281. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Annino, L., Di Giovanni, S., Tentori, L. Jr et al. (1984). Acquired hemoglobin H disease in a case of refractory anemia with excess of blasts (RAEB) evolving into acute nonlymphoid leukemia. Acta Haematol. 72, 41. CrossrefCASPubMedWeb of Science®Google Scholar Anoussakis, C., Alexiou, D., Abatxis, D. & Bechrakis, G. (1977) Endocrinological investigation of pituitary gonadal axis in thalas-saemia major. Acta Paediatr. Scand. 66, 49. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Antonarakis, S.E., Boehm, C.D., Giardina, P.V.J. & Kazazian, H.H. (1982) Non random association of polymorphic restriction sites in the β-globin gene complex. Proc. Natl Acad. Sci. USA 79, 137. CrossrefCASPubMedWeb of Science®Google Scholar Antonarakis, S.E., Orkin, S.H., Cheng, T.-C. et al. (1984) β-Thalassemia in American blacks: novel mutations in the TATA box and IVS-2 acceptor splice site. Proc. Natl Acad. Sci. USA 81, 1154. CrossrefCASPubMedWeb of Science®Google Scholar Antonarakis, S.E., Kang, J., Lam, V.M.S., Tam, J.W.O. & Li, A.M.C. (1988) Molecular characterization of β-globin gene mutations in patients with β-thalassemia intermedia in South China. Br. J. Haematol. 70, 357. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Antoniou, M. & Grosveld, F. (1990) The β-globin dominant control region interacts differently with distal and proximal promoter elements. Genes Dev. 4, 1007. CrossrefCASPubMedWeb of Science®Google Scholar Antoniou, M., deBoer, E., Habets, G. & Grosveld, F. (1988) The human β-globin gene contains multiple regulatory regions: identi-fication of one promoter and two downstream enhancers. EMBO J. 7, 377. Wiley Online LibraryCASPubMedWeb of Science®Google Scholar Anuwatanakulchia, M., Pootraku" @default.
• W4205981346 created "2022-01-26" @default.
• W4205981346 date "2001-01-01" @default.
• W4205981346 modified "2023-09-23" @default.
• W4205981346 title "References" @default.
• W4205981346 cites W106161836 @default.
• W4205981346 cites W108640602 @default.
• W4205981346 cites W110138022 @default.
• W4205981346 cites W113104820 @default.
• W4205981346 cites W118528650 @default.
• W4205981346 cites W1214455787 @default.
• W4205981346 cites W125754261 @default.
• W4205981346 cites W1277787372 @default.
• W4205981346 cites W14286575 @default.
• W4205981346 cites W1483706865 @default.
• W4205981346 cites W1488899745 @default.
• W4205981346 cites W1493884516 @default.
• W4205981346 cites W1498035654 @default.
• W4205981346 cites W1499356069 @default.
• W4205981346 cites W1503045649 @default.
• W4205981346 cites W1508246134 @default.
• W4205981346 cites W1511176131 @default.
• W4205981346 cites W1514116797 @default.
• W4205981346 cites W1514932744 @default.
• W4205981346 cites W1518415464 @default.
• W4205981346 cites W1518495327 @default.
• W4205981346 cites W1518878478 @default.
• W4205981346 cites W1520712994 @default.
• W4205981346 cites W1523189772 @default.
• W4205981346 cites W1528512169 @default.
• W4205981346 cites W1529636111 @default.
• W4205981346 cites W1529638263 @default.
• W4205981346 cites W1531301657 @default.
• W4205981346 cites W1537569102 @default.
• W4205981346 cites W1537630881 @default.
• W4205981346 cites W1543208599 @default.
• W4205981346 cites W1547032457 @default.
• W4205981346 cites W1547680166 @default.
• W4205981346 cites W1551136355 @default.
• W4205981346 cites W1554616150 @default.
• W4205981346 cites W1555921511 @default.
• W4205981346 cites W1556432187 @default.
• W4205981346 cites W1559307951 @default.
• W4205981346 cites W1565813060 @default.
• W4205981346 cites W1565858755 @default.
• W4205981346 cites W1569553189 @default.
• W4205981346 cites W1571450628 @default.
• W4205981346 cites W1572908352 @default.
• W4205981346 cites W1578477650 @default.
• W4205981346 cites W1579613226 @default.
• W4205981346 cites W1580436909 @default.
• W4205981346 cites W1586840645 @default.
• W4205981346 cites W1588496145 @default.
• W4205981346 cites W1589126424 @default.
• W4205981346 cites W1591838906 @default.
• W4205981346 cites W1595583901 @default.
• W4205981346 cites W1599673581 @default.
• W4205981346 cites W1601284278 @default.
• W4205981346 cites W1606413960 @default.
• W4205981346 cites W1612816675 @default.
• W4205981346 cites W1619099205 @default.
• W4205981346 cites W16228081 @default.
• W4205981346 cites W1627991013 @default.
• W4205981346 cites W1641090741 @default.
• W4205981346 cites W1650227569 @default.
• W4205981346 cites W1693240140 @default.
• W4205981346 cites W1714683344 @default.
• W4205981346 cites W1719867626 @default.
• W4205981346 cites W172498270 @default.
• W4205981346 cites W1731271904 @default.
• W4205981346 cites W1748211809 @default.
• W4205981346 cites W1751628521 @default.
• W4205981346 cites W1763021161 @default.
• W4205981346 cites W1775372295 @default.
• W4205981346 cites W1778216591 @default.
• W4205981346 cites W1778955668 @default.
• W4205981346 cites W1790393160 @default.
• W4205981346 cites W182013762 @default.
• W4205981346 cites W1821914260 @default.
• W4205981346 cites W182584870 @default.
• W4205981346 cites W1862820015 @default.
• W4205981346 cites W1867922214 @default.
• W4205981346 cites W1868392413 @default.
• W4205981346 cites W1877124491 @default.
• W4205981346 cites W188488539 @default.
• W4205981346 cites W1887575424 @default.
• W4205981346 cites W1894570532 @default.
• W4205981346 cites W1899172460 @default.
• W4205981346 cites W1899577620 @default.
• W4205981346 cites W1901933721 @default.
• W4205981346 cites W190417902 @default.
• W4205981346 cites W1932243120 @default.
• W4205981346 cites W1939898874 @default.
• W4205981346 cites W1963642464 @default.
• W4205981346 cites W1963787703 @default.
• W4205981346 cites W1964059575 @default.
• W4205981346 cites W196414394 @default.
• W4205981346 cites W1964439677 @default.

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