메뉴 건너뛰기




Volumn 27, Issue 3, 2003, Pages 235-242

Clonal cytogenetic abnormalities in bone marrow specimens without clear morphologic evidence of dysplasia: A form fruste of myelodysplasia?

Author keywords

Bone marrow morphology; Cytogenetics; Cytopenias; Myelodysplasia

Indexed keywords

ACUTE GRANULOCYTIC LEUKEMIA; ADULT; AGED; ARTICLE; BONE MARROW CELL; BONE MARROW EXAMINATION; CHROMOSOME 13Q; CHROMOSOME 20Q; CHROMOSOME 5Q; CHROMOSOME 7; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; CLINICAL FEATURE; CLONAL VARIATION; CYTOPENIA; DEATH; DISEASE COURSE; FEMALE; FOLLOW UP; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; KARYOTYPE; LYMPHOPROLIFERATIVE DISEASE; MAJOR CLINICAL STUDY; MALE; MONOSOMY; MYELODYSPLASIA; PLASMA CELL DYSCRASIA; PRIORITY JOURNAL; PROGNOSIS;

EID: 0037353282     PISSN: 01452126     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0145-2126(02)00161-3     Document Type: Article
Times cited : (59)

References (74)
  • 1
    • 0034054939 scopus 로고    scopus 로고
    • Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes, Grupo Cooperativo Espanol de Citogenetica Hematologica
    • Sole F., Espinet B., Sanz G.F., Cervera J., Calasanz M.J., Luno E.et al. Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes, Grupo Cooperativo Espanol de Citogenetica Hematologica. Br J. Haematol. 108:2000;346-356.
    • (2000) Br J. Haematol. , vol.108 , pp. 346-356
    • Sole, F.1    Espinet, B.2    Sanz, G.F.3    Cervera, J.4    Calasanz, M.J.5    Luno, E.6
  • 4
    • 0026536685 scopus 로고
    • Chromosomal deletions in the myelodysplastic syndrome
    • Mufti G.J. Chromosomal deletions in the myelodysplastic syndrome. Leuk. Res. 16:1992;35-41.
    • (1992) Leuk. Res. , vol.16 , pp. 35-41
    • Mufti, G.J.1
  • 5
    • 0034988764 scopus 로고    scopus 로고
    • Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia
    • Tefferi A., Mesa R.A., Schroeder G., Hanson C.A., Li C.Y., Dewald G.W. Cytogenetic findings and their clinical relevance in myelofibrosis with myeloid metaplasia. Br. J. Haematol. 113:2001;763-771.
    • (2001) Br. J. Haematol. , vol.113 , pp. 763-771
    • Tefferi, A.1    Mesa, R.A.2    Schroeder, G.3    Hanson, C.A.4    Li, C.Y.5    Dewald, G.W.6
  • 6
    • 0029154197 scopus 로고
    • Chromosome abnormalities in the myeloproliferative disorders
    • Dewald G.W., Wright P.I. Chromosome abnormalities in the myeloproliferative disorders. Semin. Oncol. 22:1995;341-354.
    • (1995) Semin. Oncol. , vol.22 , pp. 341-354
    • Dewald, G.W.1    Wright, P.I.2
  • 10
    • 0032784783 scopus 로고    scopus 로고
    • World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: Report of the Clinical Advisory Committee meeting-Airlie House, Virginia, November 1997
    • Harris N.L., Jaffe E.S., Diebold J., Flandrin G., Muller-Hermelink H.K., Vardiman J.et al. World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: report of the Clinical Advisory Committee meeting-Airlie House, Virginia, November 1997. J. Clin. Oncol. 17:1999;3835-3849.
    • (1999) J. Clin. Oncol. , vol.17 , pp. 3835-3849
    • Harris, N.L.1    Jaffe, E.S.2    Diebold, J.3    Flandrin, G.4    Muller-Hermelink, H.K.5    Vardiman, J.6
  • 11
    • 0031902192 scopus 로고    scopus 로고
    • Chromosomal abnormalities and molecular genetics of non-Hodgkin's lymphoma
    • Ong S.T., Le Beau M.M. Chromosomal abnormalities and molecular genetics of non-Hodgkin's lymphoma. Semin. Oncol. 25:1998;447-460.
    • (1998) Semin. Oncol. , vol.25 , pp. 447-460
    • Ong, S.T.1    Le Beau, M.M.2
  • 13
    • 0026669997 scopus 로고
    • Loss of the Y chromosome from normal and neoplastic bone marrows
    • United Kingdom Cancer Cytogenetics Group (UKCCG)
    • Loss of the Y chromosome from normal and neoplastic bone marrows. United Kingdom Cancer Cytogenetics Group (UKCCG). Genes Chromosomes Cancer 1992;5:83-8.
    • (1992) Genes Chromosomes Cancer , vol.5 , pp. 83-88
  • 14
    • 0033066538 scopus 로고    scopus 로고
    • Loss of the Y chromosome in bone marrow cells: Results on 1907 consecutive cases of leukaemia and preleukaemia
    • Herens C., Brasseur E., Jamar M., Vierset L., Schoenen I., Koulischer L. Loss of the Y chromosome in bone marrow cells: results on 1907 consecutive cases of leukaemia and preleukaemia. Clin. Lab. Haematol. 21:1999;17-20.
    • (1999) Clin. Lab. Haematol. , vol.21 , pp. 17-20
    • Herens, C.1    Brasseur, E.2    Jamar, M.3    Vierset, L.4    Schoenen, I.5    Koulischer, L.6
  • 15
    • 0015416999 scopus 로고
    • Age-associated aneuploidy: Loss of Y chromosome from human bone marrow cells with aging
    • Pierre R.V., Hoagland H.C. Age-associated aneuploidy: loss of Y chromosome from human bone marrow cells with aging. Cancer. 30:1972;889-894.
    • (1972) Cancer , vol.30 , pp. 889-894
    • Pierre, R.V.1    Hoagland, H.C.2
  • 16
    • 0023525879 scopus 로고
    • Clonal cytogenetic abnormalities in patients with otherwise typical aplastic anemia
    • Appelbaum F.R., Barrall J., Storb R., Ramberg R., Doney K., Sale G.E.et al. Clonal cytogenetic abnormalities in patients with otherwise typical aplastic anemia. Exp. Hematol. 15:1987;1134-1139.
    • (1987) Exp. Hematol. , vol.15 , pp. 1134-1139
    • Appelbaum, F.R.1    Barrall, J.2    Storb, R.3    Ramberg, R.4    Doney, K.5    Sale, G.E.6
  • 17
    • 0023881064 scopus 로고
    • Culturing and robotic harvesting of bone marrow, lymph nodes, peripheral blood, fibroblasts, and solid tumors with in situ techniques
    • Spurbeck J.L., Carlson R.O., Allen J.E., Dewald G.W. Culturing and robotic harvesting of bone marrow, lymph nodes, peripheral blood, fibroblasts, and solid tumors with in situ techniques. Cancer Genet. Cytogenet. 32:1988;59-66.
    • (1988) Cancer Genet. Cytogenet. , vol.32 , pp. 59-66
    • Spurbeck, J.L.1    Carlson, R.O.2    Allen, J.E.3    Dewald, G.W.4
  • 19
    • 0027725137 scopus 로고
    • PG-M1: A new monoclonal antibody directed against a fixative-resistant epitope on the macrophage-restricted form of the CD68 molecule
    • Falini B., Flenghi L., Pileri S., Gambacorta M., Bigerna B., Durkop H.et al. PG-M1: a new monoclonal antibody directed against a fixative-resistant epitope on the macrophage-restricted form of the CD68 molecule. Am. J. Pathol. 142:1993;1359-1372.
    • (1993) Am. J. Pathol. , vol.142 , pp. 1359-1372
    • Falini, B.1    Flenghi, L.2    Pileri, S.3    Gambacorta, M.4    Bigerna, B.5    Durkop, H.6
  • 20
    • 0032854508 scopus 로고    scopus 로고
    • Bone marrow effects of anagrelide therapy in patients with myelofibrosis with myeloid metaplasia
    • Yoon S.Y., Li C.Y., Mesa R.A., Tefferi A. Bone marrow effects of anagrelide therapy in patients with myelofibrosis with myeloid metaplasia. Br. J. Haematol. 106:1999;682-688.
    • (1999) Br. J. Haematol. , vol.106 , pp. 682-688
    • Yoon, S.Y.1    Li, C.Y.2    Mesa, R.A.3    Tefferi, A.4
  • 21
    • 4243895778 scopus 로고    scopus 로고
    • Clonal T-cell and immunoglobulin gene rearrangements in myelodysplastic syndromes (MDS): A morphologic and immunoperoxidase study
    • Hanson C.A., Dayharsh G.A., Morice W.G., Hodnefield J.M., Steensma D.P. Clonal T-cell and immunoglobulin gene rearrangements in myelodysplastic syndromes (MDS): a morphologic and immunoperoxidase study. Leuk. Res. 25:2001;S12-S13.
    • (2001) Leuk. Res. , vol.25 , pp. 12-S13
    • Hanson, C.A.1    Dayharsh, G.A.2    Morice, W.G.3    Hodnefield, J.M.4    Steensma, D.P.5
  • 24
    • 0033995780 scopus 로고    scopus 로고
    • 154 Chromosome anomalies in hematologic malignancies
    • Dewald G.W., Stupca P. 154 chromosome anomalies in hematologic malignancies. Leuk. Res. 24:2000;487-489.
    • (2000) Leuk. Res. , vol.24 , pp. 487-489
    • Dewald, G.W.1    Stupca, P.2
  • 25
    • 0022645855 scopus 로고
    • Unbalanced 1;7 translocation and therapy-induced hematologic disorders: A possible relationship
    • Morrison-DeLap S.J., Kuffel D.G., Dewald G.W., Letendre L. Unbalanced 1;7 translocation and therapy-induced hematologic disorders: a possible relationship. Am. J. Hematol. 21:1986;39-47.
    • (1986) Am. J. Hematol. , vol.21 , pp. 39-47
    • Morrison-DeLap, S.J.1    Kuffel, D.G.2    Dewald, G.W.3    Letendre, L.4
  • 26
    • 0031730137 scopus 로고    scopus 로고
    • Myelodysplastic syndrome (MDS) with unbalanced t(1;7) after severe aplastic anemia (SAA) in childhood as a variant form of monosomy 7
    • Kikuchi A., Ohashi H., Hanada R., Yamamoto K. Myelodysplastic syndrome (MDS) with unbalanced t(1;7) after severe aplastic anemia (SAA) in childhood as a variant form of monosomy 7. Leukemia. 12:1998;2036-2038.
    • (1998) Leukemia , vol.12 , pp. 2036-2038
    • Kikuchi, A.1    Ohashi, H.2    Hanada, R.3    Yamamoto, K.4
  • 27
    • 0021254497 scopus 로고
    • Hematologic manifestations associated with deletions of the long arm of chromosome 20
    • Davis M.P., Dewald G.W., Pierre R.V., Hoagland H.C. Hematologic manifestations associated with deletions of the long arm of chromosome 20. Cancer Genet. Cytogenet. 12:1984;63-71.
    • (1984) Cancer Genet. Cytogenet. , vol.12 , pp. 63-71
    • Davis, M.P.1    Dewald, G.W.2    Pierre, R.V.3    Hoagland, H.C.4
  • 28
    • 0027458441 scopus 로고
    • The 5q-syndrome: A single-institution study of 43 consecutive patients
    • Mathew P., Tefferi A., Dewald G.W., Goldberg S.L., Su J., Hoagland H.C.et al. The 5q-syndrome: a single-institution study of 43 consecutive patients. Blood. 81:1993;1040-1045.
    • (1993) Blood , vol.81 , pp. 1040-1045
    • Mathew, P.1    Tefferi, A.2    Dewald, G.W.3    Goldberg, S.L.4    Su, J.5    Hoagland, H.C.6
  • 29
    • 0030897009 scopus 로고    scopus 로고
    • International scoring system for evaluating prognosis in myelodysplastic syndromes
    • Greenberg P., Cox C., LeBeau M.M., Fenaux P., Morel P., Sanz G.et al. International scoring system for evaluating prognosis in myelodysplastic syndromes. Blood. 89:1997;2079-2088.
    • (1997) Blood , vol.89 , pp. 2079-2088
    • Greenberg, P.1    Cox, C.2    LeBeau, M.M.3    Fenaux, P.4    Morel, P.5    Sanz, G.6
  • 30
    • 0031975407 scopus 로고    scopus 로고
    • Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies
    • La Starza R., Wlodarska I., Aventin A., Falzetti D., Crescenzi B., Martelli M.F.et al. Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies. Blood. 91:1998;231-237.
    • (1998) Blood , vol.91 , pp. 231-237
    • La Starza, R.1    Wlodarska, I.2    Aventin, A.3    Falzetti, D.4    Crescenzi, B.5    Martelli, M.F.6
  • 31
    • 0036197441 scopus 로고    scopus 로고
    • Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: Report from an International Workshop
    • Olney H.J., Mitelman F., Johansson B., Mrozek K., Berger R., Rowley J.D. Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: report from an International Workshop. Genes Chromosomes Cancer. 33:2002;413-423.
    • (2002) Genes Chromosomes Cancer , vol.33 , pp. 413-423
    • Olney, H.J.1    Mitelman, F.2    Johansson, B.3    Mrozek, K.4    Berger, R.5    Rowley, J.D.6
  • 32
    • 0036194105 scopus 로고    scopus 로고
    • Rare recurring balanced chromosome abnormalities in therapy-related myelodysplastic syndromes and acute leukemia: Report from an International Workshop
    • Block A.W., Carroll A.J., Hagemeijer A., Lm L.M., van Lom K., Olney H.J.et al. Rare recurring balanced chromosome abnormalities in therapy-related myelodysplastic syndromes and acute leukemia: report from an International Workshop. Genes Chromosomes Cancer. 33:2002;401-412.
    • (2002) Genes Chromosomes Cancer , vol.33 , pp. 401-412
    • Block, A.W.1    Carroll, A.J.2    Hagemeijer, A.3    Lm, L.M.4    Van Lom, K.5    Olney, H.J.6
  • 34
    • 0027286442 scopus 로고
    • Issues in the pathology and diagnosis of the chronic myeloproliferative disorders and the myelodysplastic syndromes
    • Dickstein J.I., Vardiman J.W. Issues in the pathology and diagnosis of the chronic myeloproliferative disorders and the myelodysplastic syndromes. Am. J. Clin. Pathol. 99:1993;513-525.
    • (1993) Am. J. Clin. Pathol. , vol.99 , pp. 513-525
    • Dickstein, J.I.1    Vardiman, J.W.2
  • 36
    • 0034305979 scopus 로고    scopus 로고
    • Problematic WHO reclassification of myelodysplastic syndromes: Members of the International MDS Study Group
    • Greenberg P., Anderson J., de Witte T., Estey E., Fenaux P., Gupta P.et al. Problematic WHO reclassification of myelodysplastic syndromes: members of the International MDS Study Group. J. Clin. Oncol. 18:2000;3447-3452.
    • (2000) J. Clin. Oncol. , vol.18 , pp. 3447-3452
    • Greenberg, P.1    Anderson, J.2    De Witte, T.3    Estey, E.4    Fenaux, P.5    Gupta, P.6
  • 37
    • 0026580044 scopus 로고
    • Minimal diagnostic criteria for the myelodysplastic syndrome in clinical practice
    • Tricot G.J. Minimal diagnostic criteria for the myelodysplastic syndrome in clinical practice. Leuk. Res. 16:1992;5-6.
    • (1992) Leuk. Res. , vol.16 , pp. 5-6
    • Tricot, G.J.1
  • 38
    • 0034472615 scopus 로고    scopus 로고
    • Myelodysplasia or myeloneoplasia: Thoughts on the nosology of clonal myeloid diseases
    • Lichtman M.A. Myelodysplasia or myeloneoplasia: thoughts on the nosology of clonal myeloid diseases. Blood Cells Mol. Dis. 26:2000;572-581.
    • (2000) Blood Cells Mol. Dis. , vol.26 , pp. 572-581
    • Lichtman, M.A.1
  • 39
    • 0026077438 scopus 로고
    • Normal cytogenetic values for bone marrow based on studies of bone marrow transplant donors
    • Kuffel D.G., Schultz C.G., Ash R.C., Dewald G.W. Normal cytogenetic values for bone marrow based on studies of bone marrow transplant donors. Cancer Genet. Cytogenet. 55:1991;39-48.
    • (1991) Cancer Genet. Cytogenet. , vol.55 , pp. 39-48
    • Kuffel, D.G.1    Schultz, C.G.2    Ash, R.C.3    Dewald, G.W.4
  • 40
    • 0028091121 scopus 로고
    • Recurrent cytogenetic abnormalities observed in complete remission of acute myeloid leukemia do not necessarily mark preleukemic cells
    • Raynaud S.D., Brunet B., Chischportich M., Bayle J., Gratecos N., Pesce A.et al. Recurrent cytogenetic abnormalities observed in complete remission of acute myeloid leukemia do not necessarily mark preleukemic cells. Leukemia. 8:1994;245-249.
    • (1994) Leukemia , vol.8 , pp. 245-249
    • Raynaud, S.D.1    Brunet, B.2    Chischportich, M.3    Bayle, J.4    Gratecos, N.5    Pesce, A.6
  • 41
    • 13044312738 scopus 로고    scopus 로고
    • Detection of abnormal pretransplant clones in progenitor cells of patients who developed myelodysplasia after autologous transplantation
    • Abruzzese E., Radford J.E., Miller J.S., Vredenburgh J.J., Rao P.N., Pettenati M.J.et al. Detection of abnormal pretransplant clones in progenitor cells of patients who developed myelodysplasia after autologous transplantation. Blood. 94:1999;1814-1819.
    • (1999) Blood , vol.94 , pp. 1814-1819
    • Abruzzese, E.1    Radford, J.E.2    Miller, J.S.3    Vredenburgh, J.J.4    Rao, P.N.5    Pettenati, M.J.6
  • 42
    • 0021365147 scopus 로고
    • Recurrent chromosomal defects are found in most patients with acute non-lymphocytic leukemia
    • Yunis J.J. Recurrent chromosomal defects are found in most patients with acute non-lymphocytic leukemia. Cancer Genet. Cytogenet. 11:1984;125-137.
    • (1984) Cancer Genet. Cytogenet. , vol.11 , pp. 125-137
    • Yunis, J.J.1
  • 44
    • 0035124250 scopus 로고    scopus 로고
    • Three cases of typical aplastic anemia associated with a Philadelphia chromosome
    • Suzan F., Terre C., Garcia I., Bastie J., Baumelou E., Gluckman E.et al. Three cases of typical aplastic anemia associated with a Philadelphia chromosome. Br. J. Haematol. 112:2001;385-387.
    • (2001) Br. J. Haematol. , vol.112 , pp. 385-387
    • Suzan, F.1    Terre, C.2    Garcia, I.3    Bastie, J.4    Baumelou, E.5    Gluckman, E.6
  • 47
    • 0028234052 scopus 로고
    • Myelodysplasia in a patient with preexisting paroxysmal nocturnal haemoglobinuria: A clonal disease originating from within a clonal disease
    • Longo L., Bessler M., Beris P., Swirsky D., Luzzatto L. Myelodysplasia in a patient with preexisting paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease. Br. J. Haematol. 87:1994;401-403.
    • (1994) Br. J. Haematol. , vol.87 , pp. 401-403
    • Longo, L.1    Bessler, M.2    Beris, P.3    Swirsky, D.4    Luzzatto, L.5
  • 48
    • 0028229227 scopus 로고
    • Myelodysplasia following paroxysmal nocturnal haemoglobinuria: Evidence for the emergence of a separate clone
    • van Kamp H., Smit J.W., van den Berg E., Ruud Halie M., Vellenga E. Myelodysplasia following paroxysmal nocturnal haemoglobinuria: evidence for the emergence of a separate clone. Br. J. Haematol. 87:1994;399-400.
    • (1994) Br. J. Haematol. , vol.87 , pp. 399-400
    • Van Kamp, H.1    Smit, J.W.2    Van den Berg, E.3    Ruud Halie, M.4    Vellenga, E.5
  • 49
    • 0029790993 scopus 로고    scopus 로고
    • Myelodysplasia following aplastic anemia-paroxysmal nocturnal haemoglobinuria syndrome after treatment with immunosuppression and G-CSF: Evidence for the emergence of a separate clone
    • Jin J.Y., Tooze J.A., Marsh J.C., Matthey F., Gordon-Smith E.C. Myelodysplasia following aplastic anemia-paroxysmal nocturnal haemoglobinuria syndrome after treatment with immunosuppression and G-CSF: evidence for the emergence of a separate clone. Br. J. Haematol. 94:1996;510-512.
    • (1996) Br. J. Haematol. , vol.94 , pp. 510-512
    • Jin, J.Y.1    Tooze, J.A.2    Marsh, J.C.3    Matthey, F.4    Gordon-Smith, E.C.5
  • 50
    • 0034048199 scopus 로고    scopus 로고
    • Myelodysplastic syndrome and aplastic anemia-diagnostic and conceptual uncertainties
    • Barrett J. Myelodysplastic syndrome and aplastic anemia-diagnostic and conceptual uncertainties. Leuk. Res. 24:2000;595-596.
    • (2000) Leuk. Res. , vol.24 , pp. 595-596
    • Barrett, J.1
  • 51
    • 0029846342 scopus 로고    scopus 로고
    • Hematologic disorders associated with deletions of chromosome 20q: A clinicopathologic study of 107 patients
    • Kurtin P.J., Dewald G.W., Shields D.J., Hanson C.A. Hematologic disorders associated with deletions of chromosome 20q: a clinicopathologic study of 107 patients. Am. J. Clin. Pathol. 106:1996;680-688.
    • (1996) Am. J. Clin. Pathol. , vol.106 , pp. 680-688
    • Kurtin, P.J.1    Dewald, G.W.2    Shields, D.J.3    Hanson, C.A.4
  • 52
    • 0028871987 scopus 로고
    • Different genetic pathways in leukemogenesis for patients presenting with therapy-related myelodysplasia and therapy-related acute myeloid leukemia
    • Pedersen-Bjergaard J., Pedersen M., Roulston D., Philip P. Different genetic pathways in leukemogenesis for patients presenting with therapy-related myelodysplasia and therapy-related acute myeloid leukemia. Blood. 86:1995;3542-3552.
    • (1995) Blood , vol.86 , pp. 3542-3552
    • Pedersen-Bjergaard, J.1    Pedersen, M.2    Roulston, D.3    Philip, P.4
  • 53
    • 0020056752 scopus 로고
    • Thrombocytopenia as presenting symptom of preleukaemia in three patients
    • Tricot G., Criel A., Verwilghen R.L. Thrombocytopenia as presenting symptom of preleukaemia in three patients. Scand. J. Haematol. 28:1982;243-250.
    • (1982) Scand. J. Haematol. , vol.28 , pp. 243-250
    • Tricot, G.1    Criel, A.2    Verwilghen, R.L.3
  • 55
    • 8944225498 scopus 로고    scopus 로고
    • Idiopathic thrombocytopenic purpura: A practice guideline developed by explicit methods for the American Society of Hematology
    • George J.N., Woolf S.H., Raskob G.E., Wasser J.S., Aledort L.M., Ballem P.J.et al. Idiopathic thrombocytopenic purpura: a practice guideline developed by explicit methods for the American Society of Hematology. Blood. 88:1996;3-40.
    • (1996) Blood , vol.88 , pp. 3-40
    • George, J.N.1    Woolf, S.H.2    Raskob, G.E.3    Wasser, J.S.4    Aledort, L.M.5    Ballem, P.J.6
  • 56
    • 0024423204 scopus 로고
    • Refractory anemia with excess of blasts in transformation hematologic and clinical study of 52 patients
    • Michels S.D., Saumur J., Arthur D.C., Robison L.L., Brunning R.D. Refractory anemia with excess of blasts in transformation hematologic and clinical study of 52 patients. Cancer. 64:1989;2340-2346.
    • (1989) Cancer , vol.64 , pp. 2340-2346
    • Michels, S.D.1    Saumur, J.2    Arthur, D.C.3    Robison, L.L.4    Brunning, R.D.5
  • 57
    • 0028365777 scopus 로고
    • Trisomy 6 as the sole chromosome abnormality in myeloid disorders
    • Jonveaux P., Fenaux P., Berger R. Trisomy 6 as the sole chromosome abnormality in myeloid disorders. Cancer Genet. Cytogenet. 74:1994;150-152.
    • (1994) Cancer Genet. Cytogenet. , vol.74 , pp. 150-152
    • Jonveaux, P.1    Fenaux, P.2    Berger, R.3
  • 58
    • 0035863018 scopus 로고    scopus 로고
    • Trisomy 14 in myeloid malignancies: Report of two cases and review of the literature
    • Horton Y.M., Johnson P.R. Trisomy 14 in myeloid malignancies: report of two cases and review of the literature. Cancer Genet. Cytogenet. 124:2001;172-174.
    • (2001) Cancer Genet. Cytogenet. , vol.124 , pp. 172-174
    • Horton, Y.M.1    Johnson, P.R.2
  • 59
    • 0033787922 scopus 로고    scopus 로고
    • Trisomy 15 is frequently observed as a minor clone in patients with anemia/MDS/NHL and as a major clone in patients with AML
    • Batanian J.R., Slovak M.L., Mohamed A., Dobin S., Luthardt F.W., Keitges E.A. Trisomy 15 is frequently observed as a minor clone in patients with anemia/MDS/NHL and as a major clone in patients with AML. Cancer Genet. Cytogenet. 121:2000;186-189.
    • (2000) Cancer Genet. Cytogenet. , vol.121 , pp. 186-189
    • Batanian, J.R.1    Slovak, M.L.2    Mohamed, A.3    Dobin, S.4    Luthardt, F.W.5    Keitges, E.A.6
  • 60
    • 0025166263 scopus 로고
    • Clonal karyotype abnormalities and clinical progress in the myelodysplastic syndrome
    • Geddes A.A., Bowen D.T., Jacobs A. Clonal karyotype abnormalities and clinical progress in the myelodysplastic syndrome. Br. J. Haematol. 76:1990;194-202.
    • (1990) Br. J. Haematol. , vol.76 , pp. 194-202
    • Geddes, A.A.1    Bowen, D.T.2    Jacobs, A.3
  • 61
    • 0021879865 scopus 로고
    • Major karyotypic abnormalities in a near-tetraploid erythroleukemia
    • Kocova M.J., Sandberg A.A. Major karyotypic abnormalities in a near-tetraploid erythroleukemia. Cancer Genet. Cytogenet. 17:1985;143-150.
    • (1985) Cancer Genet. Cytogenet. , vol.17 , pp. 143-150
    • Kocova, M.J.1    Sandberg, A.A.2
  • 62
    • 0032188805 scopus 로고    scopus 로고
    • The importance of diagnostic cytogenetics on outcome in AML: Analysis of 1612 patients entered into the MRC AML 10 trial, The Medical Research Council Adult and Children's Leukaemia Working Parties
    • Grimwade D., Walker H., Oliver F., Wheatley K., Harrison C., Harrison G.et al. The importance of diagnostic cytogenetics on outcome in AML: analysis of 1612 patients entered into the MRC AML 10 trial, The Medical Research Council Adult and Children's Leukaemia Working Parties. Blood. 92:1998;2322-2333.
    • (1998) Blood , vol.92 , pp. 2322-2333
    • Grimwade, D.1    Walker, H.2    Oliver, F.3    Wheatley, K.4    Harrison, C.5    Harrison, G.6
  • 63
    • 0028609646 scopus 로고
    • Interstitial 9q-deletion in a case of acute myeloid leukemia-M2 arising from a granulocytic sarcoma
    • Lunde J.H., Allen E.F. Interstitial 9q-deletion in a case of acute myeloid leukemia-M2 arising from a granulocytic sarcoma. Cancer Genet. Cytogenet. 78:1994;239-241.
    • (1994) Cancer Genet. Cytogenet. , vol.78 , pp. 239-241
    • Lunde, J.H.1    Allen, E.F.2
  • 64
  • 67
    • 0026703970 scopus 로고
    • Chromosome analyses in patients with myelodysplastic syndromes: Correlation with bone marrow histopathology and prognostic significance
    • Werner M., Maschek H., Kaloutsi V., Choritz H., Georgii A. Chromosome analyses in patients with myelodysplastic syndromes: correlation with bone marrow histopathology and prognostic significance. Virchows Arch. A Pathol. Anat. Histopathol. 421:1992;47-52.
    • (1992) Virchows Arch. A Pathol. Anat. Histopathol. , vol.421 , pp. 47-52
    • Werner, M.1    Maschek, H.2    Kaloutsi, V.3    Choritz, H.4    Georgii, A.5
  • 69
    • 0032809702 scopus 로고    scopus 로고
    • A group of previously not recognized cytogenetic abnormalities in myeloid hematological malignancies
    • Chen Z., Richkind K., Roherty S., Velasco J., Lytle C., Brothman A.R.et al. A group of previously not recognized cytogenetic abnormalities in myeloid hematological malignancies. Cancer Genet. Cytogenet. 113:1999;162-165.
    • (1999) Cancer Genet. Cytogenet. , vol.113 , pp. 162-165
    • Chen, Z.1    Richkind, K.2    Roherty, S.3    Velasco, J.4    Lytle, C.5    Brothman, A.R.6
  • 70
    • 0031945625 scopus 로고    scopus 로고
    • Secondary acute leukemia and myelodysplastic syndrome with 11q23 abnormalities: EU concerted action 11q23 workshop
    • Secker-Walker L.M., Moorman A.V., Bain B.J., Mehta A.B. Secondary acute leukemia and myelodysplastic syndrome with 11q23 abnormalities: EU concerted action 11q23 workshop. Leukemia. 12:1998;840-844.
    • (1998) Leukemia , vol.12 , pp. 840-844
    • Secker-Walker, L.M.1    Moorman, A.V.2    Bain, B.J.3    Mehta, A.B.4
  • 71
    • 0029827390 scopus 로고    scopus 로고
    • 3p21 is a recurrent treatment-related breakpoint in myelodysplastic syndrome and acute myeloid leukemia
    • Shi G., Weh H.J., Martensen S., Seeger D., Hossfeld D.K. 3p21 is a recurrent treatment-related breakpoint in myelodysplastic syndrome and acute myeloid leukemia. Cytogenet. Cell Genet. 74:1996;295-299.
    • (1996) Cytogenet. Cell Genet. , vol.74 , pp. 295-299
    • Shi, G.1    Weh, H.J.2    Martensen, S.3    Seeger, D.4    Hossfeld, D.K.5
  • 73
    • 0024423029 scopus 로고
    • Twenty-six patients with hematologic disorders and X chromosome abnormalities. Frequent idic(X)(q13) chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts
    • Dewald G.W., Brecher M., Travis L.B., Stupca P.J. Twenty-six patients with hematologic disorders and X chromosome abnormalities. Frequent idic(X)(q13) chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts. Cancer Genet. Cytogenet. 42:1989;173-185.
    • (1989) Cancer Genet. Cytogenet. , vol.42 , pp. 173-185
    • Dewald, G.W.1    Brecher, M.2    Travis, L.B.3    Stupca, P.J.4
  • 74
    • 0020053658 scopus 로고
    • Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia
    • Dewald G.W., Pierre R.V., Phyliky R.L. Three patients with structurally abnormal X chromosomes, each with Xq13 breakpoints and a history of idiopathic acquired sideroblastic anemia. Blood. 59:1982;100-105.
    • (1982) Blood , vol.59 , pp. 100-105
    • Dewald, G.W.1    Pierre, R.V.2    Phyliky, R.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.