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Volumn 24, Issue 1, 2000, Pages 79-81

Acute promyelocytic leukemia with del(6)(p23)

Author keywords

Acute promyelocytic leukemia; Del(6)(p23); Non specific esterase

Indexed keywords

ACUTE MYELOBLASTIC LEUKEMIA; AGED; ARTICLE; CASE REPORT; CHROMOSOMAL LOCALIZATION; CHROMOSOME ABERRATION; CYTOGENETICS; DISEASE ASSOCIATION; GENETIC ANALYSIS; HUMAN; KARYOTYPING; MALE; PRIORITY JOURNAL;

EID: 0033991637     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0145-2126(99)00139-3     Document Type: Article
Times cited : (12)

References (13)
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    • Matsuo, T.1    Jain, N.C.2    Bennett, J.M.3
  • 3
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    • Differing form of variant form of hypergranular promyelocytic leukaemia (M3), or transition between M3 and monocytic leukaemia
    • Stavem P., Rorvik T.O., Blichfeldt P., Hagen C.B. Differing form of variant form of hypergranular promyelocytic leukaemia (M3), or transition between M3 and monocytic leukaemia. Scand. J. Haematol. 26:1981;149.
    • (1981) Scand. J. Haematol. , vol.26 , pp. 149
    • Stavem, P.1    Rorvik, T.O.2    Blichfeldt, P.3    Hagen, C.B.4
  • 5
    • 0024516029 scopus 로고
    • Immunophenotypic and enzymatic studies do not support the concept of mixed monocytic-granulocytic differentiation in acute promyelocytic leukaemia (M3): A study of 44 cases
    • Scott C.S., Patel D., Drexler H.G., Master P.S., Limbert H.J., Roberts B.E. Immunophenotypic and enzymatic studies do not support the concept of mixed monocytic-granulocytic differentiation in acute promyelocytic leukaemia (M3): A study of 44 cases. Br. J. Haematol. 71:1989;505.
    • (1989) Br. J. Haematol. , vol.71 , pp. 505
    • Scott, C.S.1    Patel, D.2    Drexler, H.G.3    Master, P.S.4    Limbert, H.J.5    Roberts, B.E.6
  • 7
    • 0024455497 scopus 로고
    • Chromosome 6p rearrangements appear to be secondary changes in various haematological malignancies
    • Huret J.L., Schoenwald M., Brizard A., Guklhot F., Vilmer E., Tanzer J. Chromosome 6p rearrangements appear to be secondary changes in various haematological malignancies. Leuk. Res. 13:1989;819.
    • (1989) Leuk. Res. , vol.13 , pp. 819
    • Huret, J.L.1    Schoenwald, M.2    Brizard, A.3    Guklhot, F.4    Vilmer, E.5    Tanzer, J.6
  • 8
    • 0023689044 scopus 로고
    • Cytogenetics of acutely transformed chronic myeloproliferative syndromes without a Philadelphia chromosome. A multicenter study of 55 patients
    • Groupe Francais de Cytogenetique Hematologique.
    • Groupe Francais de Cytogenetique Hematologique. Cytogenetics of acutely transformed chronic myeloproliferative syndromes without a Philadelphia chromosome. A multicenter study of 55 patients, Cancer Genet. Cytogenet 1988;32:157.
    • (1988) Cancer Genet. Cytogenet , vol.32 , pp. 157
  • 11
    • 0030325303 scopus 로고    scopus 로고
    • A multimodal approach for diagnosing patients with acute promyelocytic leukemia
    • Mark H.F.L., Dong H., Forman E., Smith P., Glasser L. A multimodal approach for diagnosing patients with acute promyelocytic leukemia. Cytobiosystems. 87:1996;1996.
    • (1996) Cytobiosystems , vol.87 , pp. 1996
    • Mark, H.F.L.1    Dong, H.2    Forman, E.3    Smith, P.4    Glasser, L.5
  • 12
    • 9444225115 scopus 로고    scopus 로고
    • Establishing the presence of the t(15;17) in suspected acute promyelocytic leukaemia: Cytogenetic, molecular and PML immunofluorescence assessment of patients entered into the M.R.C. ATRA trial
    • Grimwade D., Howe K., Langabeer S., Davies L., Oliver F., Walker H., Swirsky D., Wheatley K., Goldstone A., Burnett A., Solomon E. Establishing the presence of the t(15;17) in suspected acute promyelocytic leukaemia: cytogenetic, molecular and PML immunofluorescence assessment of patients entered into the M.R.C. ATRA trial. Br. J. Haematol. 94:1996;1996.
    • (1996) Br. J. Haematol. , vol.94 , pp. 1996
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  • 13
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    • The translocation (6;9)(p23;q34) shows constant rearrangement of two genes and defines a myeloproliferative disorder with specific clinical features
    • Soekarman D., von Lindern M., Daenen S., de Jong B., Fonatsch C., Heinze B., Bartram C., Hagemeijer A., Grosveld G. The translocation (6;9)(p23;q34) shows constant rearrangement of two genes and defines a myeloproliferative disorder with specific clinical features. Blood. 79:1992;2990.
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    • Soekarman, D.1    Von Lindern, M.2    Daenen, S.3    De Jong, B.4    Fonatsch, C.5    Heinze, B.6    Bartram, C.7    Hagemeijer, A.8    Grosveld, G.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.