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Volumn 128, Issue 5, 2005, Pages 722-729

Heterogeneity of the εγδδ-thalassaemias: Characterization of three novel English deletions

Author keywords

thalassaemia; Deletion; Neonatal haemolytic anaemia

Indexed keywords

BETA GLOBIN; DELTA GLOBIN; EPSILON GLOBIN; GAMMA GLOBIN; GLOBIN; UNCLASSIFIED DRUG;

EID: 20044391420     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2005.05368.x     Document Type: Article
Times cited : (26)

References (22)
  • 7
    • 0025844863 scopus 로고
    • A >200 kb deletion removing the entire β-like globin gene cluster in a family of Irish descent
    • Fortina, P., Delgrosso, K., Werner, E., Haines, K., Rappaport, E., Schwartz, E. & Surrey, S. (1991) A >200 kb deletion removing the entire β-like globin gene cluster in a family of Irish descent. Hemoglobin, 15, 23-41.
    • (1991) Hemoglobin , vol.15 , pp. 23-41
    • Fortina, P.1    Delgrosso, K.2    Werner, E.3    Haines, K.4    Rappaport, E.5    Schwartz, E.6    Surrey, S.7
  • 9
    • 0027266979 scopus 로고
    • The regulation of human globin gene expression
    • (ed. byD.R. Higgs & D.J. Weatherall), Baillière Tindall, London
    • Grosveld, F., Dillon, N. & Higgs, D. (1993) The regulation of human globin gene expression. In: Baillière's Clinical Haematology Vol. 6:1 (ed. byD.R. Higgs & D.J. Weatherall), pp. 31-55. Baillière Tindall, London.
    • (1993) Baillière's Clinical Haematology , vol.6 , Issue.1 , pp. 31-55
    • Grosveld, F.1    Dillon, N.2    Higgs, D.3
  • 12
    • 0025349984 scopus 로고
    • Molecular analysis of deletions in the human β-globin gene cluster: Deletion junctions and locations of breakpoints
    • Henthorn, P.S., Smithies, O. & Mager, D.L. (1990) Molecular analysis of deletions in the human β-globin gene cluster: deletion junctions and locations of breakpoints. Cenomics, 6, 226-237.
    • (1990) Cenomics , vol.6 , pp. 226-237
    • Henthorn, P.S.1    Smithies, O.2    Mager, D.L.3
  • 13
    • 0015516517 scopus 로고
    • Gamma-beta thalassemia: A cause of hemolytic disease of the newborn
    • Kan, Y.W., Forget, B.C. & Nathan, D.G. (1972) Gamma-beta thalassemia: a cause of hemolytic disease of the newborn. New England Journal of Medicine, 286, 129-134 .
    • (1972) New England Journal of Medicine , vol.286 , pp. 129-134
    • Kan, Y.W.1    Forget, B.C.2    Nathan, D.G.3
  • 17
    • 0024376665 scopus 로고
    • Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes
    • Sutton, M., Bouhassira, E.E. & Nagel, R.L. (1989) Polymerase chain reaction amplification applied to the determination of β-like globin gene cluster haplotypes. American Journal of Hematology, 32, 66-69.
    • (1989) American Journal of Hematology , vol.32 , pp. 66-69
    • Sutton, M.1    Bouhassira, E.E.2    Nagel, R.L.3
  • 19
    • 0025223668 scopus 로고
    • Molecular and hematologic characterization of Scottish-Irish type (εγδβ)° thalassemia
    • Trent, R.J., Williams, B.C., Kearney, A., Wilkinson, T. & Harris, P.C. (1990) Molecular and hematologic characterization of Scottish-Irish type (εγδβ)° thalassemia. Blood, 76, 2132-2138.
    • (1990) Blood , vol.76 , pp. 2132-2138
    • Trent, R.J.1    Williams, B.C.2    Kearney, A.3    Wilkinson, T.4    Harris, P.C.5
  • 20
    • 1842344882 scopus 로고
    • Different 3′ end points of deletions causing δβ- thalassemia and hereditary persistence of fetal hemoglobin: Implications for the control of γ-globin gene expression in man
    • Tuan, D., Feingold, E., Newman, M., Weissman, S.M. & Forget, B.G. (1983) Different 3′ end points of deletions causing δβ- thalassemia and hereditary persistence of fetal hemoglobin: Implications for the control of γ-globin gene expression in man. Proceedings of the National Academy of Sciences of the United States of America, 80, 6937-6941.
    • (1983) Proceedings of the National Academy of Sciences of the United States of America , vol.80 , pp. 6937-6941
    • Tuan, D.1    Feingold, E.2    Newman, M.3    Weissman, S.M.4    Forget, B.G.5
  • 21
    • 0019223735 scopus 로고
    • γ-β-thalassaemia studies showing that deletion of the γ- And β-genes influences β-globin gene expression in man
    • Van der Ploeg, L.H.T., Konings, A., Oort, M., Roos, D., Bernini, L. & Flavell, R.A. (1980) γ-β-thalassaemia studies showing that deletion of the γ- and β-genes influences β-globin gene expression in man. Nature, 283, 637-642.
    • (1980) Nature , vol.283 , pp. 637-642
    • Van Der Ploeg, L.H.T.1    Konings, A.2    Oort, M.3    Roos, D.4    Bernini, L.5    Flavell, R.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.