메뉴 건너뛰기




Volumn 101, Issue 1, 1998, Pages 1-6

Cytogenetic and fluorescence in situ hybridization analyses of hematologic malignancies in Korea

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ACUTE LYMPHOCYTIC LEUKEMIA; ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; CHRONIC MYELOID LEUKEMIA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; KOREA; MAJOR CLINICAL STUDY; MALE; MYELODYSPLASTIC SYNDROME; PHILADELPHIA 1 CHROMOSOME; PRIORITY JOURNAL; TRISOMY;

EID: 0032005504     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-4608(97)00357-9     Document Type: Article
Times cited : (9)

References (32)
  • 3
    • 0025849153 scopus 로고
    • Geographic heterogeneity of neoplasia-associated chromosome aberrations
    • Johansson B, Mertens F (1991): Geographic heterogeneity of neoplasia-associated chromosome aberrations. Genes Chromosom Cancer 3:1-7.
    • (1991) Genes Chromosom Cancer , vol.3 , pp. 1-7
    • Johansson, B.1    Mertens, F.2
  • 4
    • 0022612696 scopus 로고
    • Geographic heterogeneity of chromosome aberrations in hematologic disorders
    • Mitelman F (1986): Geographic heterogeneity of chromosome aberrations in hematologic disorders. Cancer Genet Cytogenet 20:203-208.
    • (1986) Cancer Genet Cytogenet , vol.20 , pp. 203-208
    • Mitelman, F.1
  • 7
    • 0026651421 scopus 로고
    • New case of t(3;17)(q26;q22) as an additional change in a Philadelphia-positive chronic myelogenous leukemia acceleration
    • Mugneret F, Solary E, Favre B, Caillot D, Sidaner I, Guy H (1992): New case of t(3;17)(q26;q22) as an additional change in a Philadelphia-positive chronic myelogenous leukemia acceleration. Cancer Genet Cytogenet 60:90-92.
    • (1992) Cancer Genet Cytogenet , vol.60 , pp. 90-92
    • Mugneret, F.1    Solary, E.2    Favre, B.3    Caillot, D.4    Sidaner, I.5    Guy, H.6
  • 15
    • 0023912924 scopus 로고
    • Prognostic value of clonal chromosomal abnormalities in patients with primary myelodysplastic syndrome
    • Gyger M, Infante-Rivard C, D'Angelo G, Forest L, Lussier P (1988): Prognostic value of clonal chromosomal abnormalities in patients with primary myelodysplastic syndrome. Am J Hematol 28:13-20.
    • (1988) Am J Hematol , vol.28 , pp. 13-20
    • Gyger, M.1    Infante-Rivard, C.2    D'Angelo, G.3    Forest, L.4    Lussier, P.5
  • 17
    • 0025177064 scopus 로고
    • Results of chromosome studies and their relation to morphology, course, and prognosis in 120 patients with de novo myelodysplastic syndrome
    • Suciu S, Kuse R, Weh HJ, Hossfeld DK (1990): Results of chromosome studies and their relation to morphology, course, and prognosis in 120 patients with de novo myelodysplastic syndrome. Cancer Genet Cytogenet 44:15-26.
    • (1990) Cancer Genet Cytogenet , vol.44 , pp. 15-26
    • Suciu, S.1    Kuse, R.2    Weh, H.J.3    Hossfeld, D.K.4
  • 18
    • 0025276914 scopus 로고
    • Complex translocations in a patient with chronic myelocytic leukemia: T(9;22;17) and t(10;18;19) after two failed bone marrow transplantations
    • Menyk A, Kowal-Vern A (1990): Complex translocations in a patient with chronic myelocytic leukemia: t(9;22;17) and t(10;18;19) after two failed bone marrow transplantations. Cancer Genet Cytogenet 46:83-87.
    • (1990) Cancer Genet Cytogenet , vol.46 , pp. 83-87
    • Menyk, A.1    Kowal-Vern, A.2
  • 19
    • 0023888449 scopus 로고
    • Recommendation for a morphologic, immunologic and cytogenetic (MIC) working classification of the primary and therapy related myelodysplastic disorder
    • Third MIC Cooperative Study Group (1988): Recommendation for a morphologic, immunologic and cytogenetic (MIC) working classification of the primary and therapy related myelodysplastic disorder. Cancer Genet Cytogenet 32:1-10.
    • (1988) Cancer Genet Cytogenet , vol.32 , pp. 1-10
  • 22
    • 0027074838 scopus 로고
    • A new nonrandom chromosomal abnormality, t(2;16)(p11.2;p11.2), possibly associated with poor outcome in childhood acute lymphoblastic leukemia
    • Lowe LR, Heerema NA, Cheeva AC, Palmer CG (1992): A new nonrandom chromosomal abnormality, t(2;16)(p11.2;p11.2), possibly associated with poor outcome in childhood acute lymphoblastic leukemia. Cancer Genet Cytogenet 64:60-64.
    • (1992) Cancer Genet Cytogenet , vol.64 , pp. 60-64
    • Lowe, L.R.1    Heerema, N.A.2    Cheeva, A.C.3    Palmer, C.G.4
  • 25
    • 0028043180 scopus 로고
    • Detection of minimal residual disease state in chronic myelogenous leukemia patients using fluorescence in situ hybridization
    • Amiel A, Yarconi S, Slavin S, Or R, Lorberboum-Glaski H, Feigin M, Nagler A (1994): Detection of minimal residual disease state in chronic myelogenous leukemia patients using fluorescence in situ hybridization. Cancer Genet Cytogenet 76:59-64.
    • (1994) Cancer Genet Cytogenet , vol.76 , pp. 59-64
    • Amiel, A.1    Yarconi, S.2    Slavin, S.3    Or, R.4    Lorberboum-Glaski, H.5    Feigin, M.6    Nagler, A.7
  • 26
    • 0023691590 scopus 로고
    • Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome specific library probes
    • Cremer T, Lichter P, Borden J, Ward DC, Manuelidis L (1988): Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome specific library probes. Hum Genet 80:235-246.
    • (1988) Hum Genet , vol.80 , pp. 235-246
    • Cremer, T.1    Lichter, P.2    Borden, J.3    Ward, D.C.4    Manuelidis, L.5
  • 27
    • 0025908474 scopus 로고
    • Nonradioactive in situ hybridization: A rapid approach for the identification of marker chromosomes: study of a case of acute leukemia with a Yq specific DNA probe
    • Wullich B, Morgan R, Berger C, Jarabek V, Sandberg AA (1991): Nonradioactive in situ hybridization: a rapid approach for the identification of marker chromosomes: study of a case of acute leukemia with a Yq specific DNA probe. Cancer Genet Cytogenet 52:161-172.
    • (1991) Cancer Genet Cytogenet , vol.52 , pp. 161-172
    • Wullich, B.1    Morgan, R.2    Berger, C.3    Jarabek, V.4    Sandberg, A.A.5
  • 28
    • 0026493845 scopus 로고
    • Application of fluorescence in situ hybridization in hematological disorder
    • Chen Z, Morgan R, Berger CS, Sandberg AA (1992): Application of fluorescence in situ hybridization in hematological disorder. Cancer Genet Cytogenet 63:62-69.
    • (1992) Cancer Genet Cytogenet , vol.63 , pp. 62-69
    • Chen, Z.1    Morgan, R.2    Berger, C.S.3    Sandberg, A.A.4
  • 30
    • 0024578349 scopus 로고
    • Immunophenotype-karyotype associations in acute lymphoblastic leukemia
    • Uckum FM, Gajl-Peczalska K), Provisor A), Heerema NA (1989): Immunophenotype-karyotype associations in acute lymphoblastic leukemia. Blood 73:271-280.
    • (1989) Blood , vol.73 , pp. 271-280
    • Uckum, F.M.1    Gajl-Peczalska, K.2    Provisor, A.3    Heerema, N.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.