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Volumn 95, Issue 3, 1996, Pages 524-526

A myeloproliferative disorder with eosinophilia associated with a unique translocation (3;5)

Author keywords

Eosinophilia; Myeloproliferative disorder; Translocation

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME TRANSLOCATION 3; CONTROLLED STUDY; EOSINOPHILIA; FEMALE; HUMAN; HUMAN CELL; MYELOPROLIFERATIVE DISORDER; PRIORITY JOURNAL;

EID: 0029859432     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1996.d01-1928.x     Document Type: Article
Times cited : (15)

References (12)
  • 1
    • 0029127510 scopus 로고
    • Autoimmune hemolytic anemia in a patient with idiopathic hypereosinophilia
    • Arquanti, M., Amodei, V., Foa, P. & Tedeschi, A. (1995) Autoimmune hemolytic anemia in a patient with idiopathic hypereosinophilia. American Journal of Hematology, 49, 356.
    • (1995) American Journal of Hematology , vol.49 , pp. 356
    • Arquanti, M.1    Amodei, V.2    Foa, P.3    Tedeschi, A.4
  • 2
    • 0020623050 scopus 로고
    • Partial deletion of the long arm of chromosome 16 and bone marrow eosinophilia in acute nonlymphocytic leukemia: A new association
    • Arthur, D.C. & Bloomfield, C.D. (1983) Partial deletion of the long arm of chromosome 16 and bone marrow eosinophilia in acute nonlymphocytic leukemia: a new association. Blood, 61, 994-998.
    • (1983) Blood , vol.61 , pp. 994-998
    • Arthur, D.C.1    Bloomfield, C.D.2
  • 5
    • 0027454104 scopus 로고
    • Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours
    • Friedman, E., Gejman, P.V., Martin, G.A. & McCormick, F. (1993) Nonsense mutations in the C-terminal SH2 region of the GTPase activating protein (GAP) gene in human tumours. Nature Genetics, 5, 242-247.
    • (1993) Nature Genetics , vol.5 , pp. 242-247
    • Friedman, E.1    Gejman, P.V.2    Martin, G.A.3    McCormick, F.4
  • 6
    • 0024353369 scopus 로고
    • The t(5;14) chromosomal translocation in a case of acute lymphocytic leukemia joins the interleukin-3 gene to the immunoglobulin heavy chain gene
    • Grimaldi, J.C. & Meeker, T.C. (1989) The t(5;14) chromosomal translocation in a case of acute lymphocytic leukemia joins the interleukin-3 gene to the immunoglobulin heavy chain gene. Blood, 73, 2081-2085.
    • (1989) Blood , vol.73 , pp. 2081-2085
    • Grimaldi, J.C.1    Meeker, T.C.2
  • 7
    • 0024842741 scopus 로고
    • Chromosome localization and cDNA sequence of murine and human genes for ras p21 GTPase activating protein (GAP)
    • Hsieh, C.L., Vogel, U.S., Dixon, R.A. & Francke, U. (1989) Chromosome localization and cDNA sequence of murine and human genes for ras p21 GTPase activating protein (GAP). Somatic Cell and Molecular Genetics, 15, 579-590.
    • (1989) Somatic Cell and Molecular Genetics , vol.15 , pp. 579-590
    • Hsieh, C.L.1    Vogel, U.S.2    Dixon, R.A.3    Francke, U.4
  • 8
    • 0028237102 scopus 로고
    • A case of myelodysplasia with eosinophilia having a translocation t(5;12)q31:q13 restricted to myeloid cells but not involving eosinophils
    • Jani, K., Kempski, M. & Reeves, B.R. (1994) A case of myelodysplasia with eosinophilia having a translocation t(5;12)q31:q13) restricted to myeloid cells but not involving eosinophils. British Journal of Haematology, 87, 57-60.
    • (1994) British Journal of Haematology , vol.87 , pp. 57-60
    • Jani, K.1    Kempski, M.2    Reeves, B.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.