-
1
-
-
33646300713
-
Chromosome studies on 30 Chinese patients with acute nonlymphocytic leukemia in Taiwan
-
Tienn HF, Charangn SM, Wang CH, Lee FY, Chien SH, Chen YC, Shen MC, Liu CH (1989): Chromosome studies on 30 Chinese patients with acute nonlymphocytic leukemia in Taiwan. Cancer Genet Cytogenet 39:89-97.
-
(1989)
Cancer Genet Cytogenet
, vol.39
, pp. 89-97
-
-
Tienn, H.F.1
Charangn, S.M.2
Wang, C.H.3
Lee, F.Y.4
Chien, S.H.5
Chen, Y.C.6
Shen, M.C.7
Liu, C.H.8
-
2
-
-
0026493823
-
Cytogenetic analysis of hematologic malignancies in Hong Kong
-
Chan LC, Kwong YL, Liu HW, Chan TK, Todd D, Ching LM [1992): Cytogenetic analysis of hematologic malignancies in Hong Kong. Cancer Genet Cytogenet 62:154-159.
-
(1992)
Cancer Genet Cytogenet
, vol.62
, pp. 154-159
-
-
Chan, L.C.1
Kwong, Y.L.2
Liu, H.W.3
Chan, T.K.4
Todd, D.5
Ching, L.M.6
-
3
-
-
0025849153
-
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
-
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
-
6
-
-
0027322485
-
Molecular analysis of six variant Philadelphia chromosome translocations in chronic myeloid leukemia
-
Sessarego M, Martinelli G, Chiamenti A, Defferrari R, Fugazza G, Bruzzone R, Ajimar F, Pignatti PF (1993): Molecular analysis of six variant Philadelphia chromosome translocations in chronic myeloid leukemia. Cancer Genet Cytogenet 67:50-54.
-
(1993)
Cancer Genet Cytogenet
, vol.67
, pp. 50-54
-
-
Sessarego, M.1
Martinelli, G.2
Chiamenti, A.3
Defferrari, R.4
Fugazza, G.5
Bruzzone, R.6
Ajimar, F.7
Pignatti, P.F.8
-
7
-
-
0026651421
-
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
-
8
-
-
0025811162
-
Detection of trisomy 8 in hematological disorders by in situ hybridization
-
Kibbelaar RE, Kamp H, Dreef EJ, Wessels JW, Beverstock GC, Raap GC, Fibbe WE, Ottolander GJ, Kluin PM (1991): Detection of trisomy 8 in hematological disorders by in situ hybridization. Cytogenet Cell Genet 56:132-136.
-
(1991)
Cytogenet Cell Genet
, vol.56
, pp. 132-136
-
-
Kibbelaar, R.E.1
Kamp, H.2
Dreef, E.J.3
Wessels, J.W.4
Beverstock, G.C.5
Raap, G.C.6
Fibbe, W.E.7
Ottolander, G.J.8
Kluin, P.M.9
-
9
-
-
0023095202
-
Toward a clinically relevant cytogenetic classification of acute myelogenous leukemia
-
Keating MJ, Cork A, Broach A, Smith T, Walters RS, McCredie KB, Trujillo J, Freireich EJ (1987): Toward a clinically relevant cytogenetic classification of acute myelogenous leukemia. Leukem Res 11:119-133.
-
(1987)
Leukem Res
, vol.11
, pp. 119-133
-
-
Keating, M.J.1
Cork, A.2
Broach, A.3
Smith, T.4
Walters, R.S.5
McCredie, K.B.6
Trujillo, J.7
Freireich, E.J.8
-
10
-
-
0026708926
-
AML with unusual chromosome change, translocation (15;21) and 5q in the presence of two normal chromosomes 5
-
Carrasco JL, Otero Gomez A, Garcia Miranda JL, Brito Barroso ML, Hernandez Garcia MT, Hernandez N (1992): AML with unusual chromosome change, translocation (15;21) and 5q in the presence of two normal chromosomes 5. Cancer Genet Cytogenet 61:139-141.
-
(1992)
Cancer Genet Cytogenet
, vol.61
, pp. 139-141
-
-
Carrasco, J.L.1
Otero Gomez, A.2
Garcia Miranda, J.L.3
Brito Barroso, M.L.4
Hernandez Garcia, M.T.5
Hernandez, N.6
-
11
-
-
0028050527
-
Variant t(8;21) rearrangement in acute myeloblastic leukemia of childhood
-
Gallego M, Carroll AJ, Gad GS, Pappo A, Head D, Behm F, Ravindranath Y, Raimondi SC (1994): Variant t(8;21) rearrangement in acute myeloblastic leukemia of childhood. Cancer Genet Cytogenet 75:139-144.
-
(1994)
Cancer Genet Cytogenet
, vol.75
, pp. 139-144
-
-
Gallego, M.1
Carroll, A.J.2
Gad, G.S.3
Pappo, A.4
Head, D.5
Behm, F.6
Ravindranath, Y.7
Raimondi, S.C.8
-
12
-
-
0028083312
-
Presenting characteristics of trisomy 8 as the primary cytogenetic abnormality associated with childhood acute lymphoblastic leukemia
-
Pettenati MJ, Rao N, Wofford M, Shuster JJ, Pullen DJ, Ling MP, Steuber CP, Carroll AJ (1994): Presenting characteristics of trisomy 8 as the primary cytogenetic abnormality associated with childhood acute lymphoblastic leukemia. Cancer Genet Cytogenet 75:6-10.
-
(1994)
Cancer Genet Cytogenet
, vol.75
, pp. 6-10
-
-
Pettenati, M.J.1
Rao, N.2
Wofford, M.3
Shuster, J.J.4
Pullen, D.J.5
Ling, M.P.6
Steuber, C.P.7
Carroll, A.J.8
-
13
-
-
0026519035
-
Cytogenetic survey of 80 patients with acute nonlymphocytic leukemia
-
Palka G, Calabrese G, Fiorotoni G, Stuppia L, Guanciali Franchi P, Marino M, Antonucci A, Spandano A, Torlantano G (1992): Cytogenetic survey of 80 patients with acute nonlymphocytic leukemia. Cancer Genet Cytogenet 59:45-50.
-
(1992)
Cancer Genet Cytogenet
, vol.59
, pp. 45-50
-
-
Palka, G.1
Calabrese, G.2
Fiorotoni, G.3
Stuppia, L.4
Guanciali Franchi, P.5
Marino, M.6
Antonucci, A.7
Spandano, A.8
Torlantano, G.9
-
14
-
-
0027086443
-
Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes
-
Sole F, Prieto F, Badia L, Woessner S, Florensa L, Caballin MR, Coll MD, Besses C, Sans-Sabrafen J (1992): Cytogenetic studies in 112 cases of untreated myelodysplastic syndromes. Cancer Genet Cytogenet 64:12-20.
-
(1992)
Cancer Genet Cytogenet
, vol.64
, pp. 12-20
-
-
Sole, F.1
Prieto, F.2
Badia, L.3
Woessner, S.4
Florensa, L.5
Caballin, M.R.6
Coll, M.D.7
Besses, C.8
Sans-Sabrafen, J.9
-
15
-
-
0023912924
-
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
-
16
-
-
0022538534
-
Prognostic implications of morphology and karyotype in primary myelodysplastic syndrome
-
Jacobs RJ, Cornbleet MA, Vardiman JW, Larson RA, LeBeau MM, Rowley JD (1986): Prognostic implications of morphology and karyotype in primary myelodysplastic syndrome. Blood 67:1765-1772.
-
(1986)
Blood
, vol.67
, pp. 1765-1772
-
-
Jacobs, R.J.1
Cornbleet, M.A.2
Vardiman, J.W.3
Larson, R.A.4
LeBeau, M.M.5
Rowley, J.D.6
-
17
-
-
0025177064
-
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
-
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
-
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
-
-
-
20
-
-
0023253681
-
11q-chromosome is associated with abnormal iron stores in myelodysplastic syndromes
-
Mecucci C, Van Orshoven A, Vermaelen K, Michaux J-L, Tricot G, Louwagie A, Delannoy A, Van Den Berghe H (1987): 11q-chromosome is associated with abnormal iron stores in myelodysplastic syndromes. Cancer Genet Cytogenet 27:39-44.
-
(1987)
Cancer Genet Cytogenet
, vol.27
, pp. 39-44
-
-
Mecucci, C.1
Van Orshoven, A.2
Vermaelen, K.3
Michaux, J.-L.4
Tricot, G.5
Louwagie, A.6
Delannoy, A.7
Van Den Berghe, H.8
-
21
-
-
0027943848
-
Cytogenetics and immunophenotypes of childhood acute leukemia in Hong Kong
-
Chan LC, Ha SY, Ching LM, Lee CP, Lau YL, Yuen P, Leung NK (1994): Cytogenetics and immunophenotypes of childhood acute leukemia in Hong Kong. Cancer Genet Cytogenet 76:118-124.
-
(1994)
Cancer Genet Cytogenet
, vol.76
, pp. 118-124
-
-
Chan, L.C.1
Ha, S.Y.2
Ching, L.M.3
Lee, C.P.4
Lau, Y.L.5
Yuen, P.6
Leung, N.K.7
-
22
-
-
0027074838
-
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
-
23
-
-
0027173896
-
t(8:14)(q11;q32) in acute lymphoid leukemia
-
Testoni N, Zaccaria A, Maaretinelli G, Pelliconi S, Buzzi M, Farabegoli P, Panzica G, Tura S (1993): t(8:14)(q11;q32) in acute lymphoid leukemia. Cancer Genet Cytogenet 67:55-58.
-
(1993)
Cancer Genet Cytogenet
, vol.67
, pp. 55-58
-
-
Testoni, N.1
Zaccaria, A.2
Maaretinelli, G.3
Pelliconi, S.4
Buzzi, M.5
Farabegoli, P.6
Panzica, G.7
Tura, S.8
-
24
-
-
0025081533
-
Monosomy 20: A nonrandom finding in childhood acute lymphoblastic leukemia
-
Betts DR, Kingston JE, Drey EL, Young BD, Webb D, Kaz FE, Gibbon B (1990): Monosomy 20: a nonrandom finding in childhood acute lymphoblastic leukemia. Genes Chromosom Cancer 2:182-185.
-
(1990)
Genes Chromosom Cancer
, vol.2
, pp. 182-185
-
-
Betts, D.R.1
Kingston, J.E.2
Drey, E.L.3
Young, B.D.4
Webb, D.5
Kaz, F.E.6
Gibbon, B.7
-
25
-
-
0028043180
-
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
-
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
-
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
-
29
-
-
0025190583
-
Cytogenetic studies of 44 T-cells acute lymphoblastic leukemias
-
Berger R, Le Coniat M, Vecchione D, Derre J, Chen SJ (1990): Cytogenetic studies of 44 T-cells acute lymphoblastic leukemias. Cancer Genet Cytogenet 44:69-75.
-
(1990)
Cancer Genet Cytogenet
, vol.44
, pp. 69-75
-
-
Berger, R.1
Le Coniat, M.2
Vecchione, D.3
Derre, J.4
Chen, S.J.5
-
30
-
-
0024578349
-
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
-
31
-
-
0026586569
-
Ph-positive chronic myeloid leukemia with t(8;21)(q22;q22) in blast crisis
-
Ferro MT, Steegman JL, Escribano L, Heinrichs B, Parada L, Garcia-Sagredo JM, Resino M, Cabello P, San Roman C (1992): Ph-positive chronic myeloid leukemia with t(8;21)(q22;q22) in blast crisis. Cancer Genet Cytogenet 58:96-99.
-
(1992)
Cancer Genet Cytogenet
, vol.58
, pp. 96-99
-
-
Ferro, M.T.1
Steegman, J.L.2
Escribano, L.3
Heinrichs, B.4
Parada, L.5
Garcia-Sagredo, J.M.6
Resino, M.7
Cabello, P.8
San Roman, C.9
-
32
-
-
0026771929
-
Cytogenetic study of acute lymphoblastic leukemia and correlation with immunophenotype and genotype
-
Tien HF, Wang CH, Lee FU, Liu MC, Chuang SM, Chen YC, Shen MC, Lin DT, Lin KH, Chu WM (1992): Cytogenetic study of acute lymphoblastic leukemia and correlation with immunophenotype and genotype. Cancer Genet Cytogenet 59:191-198.
-
(1992)
Cancer Genet Cytogenet
, vol.59
, pp. 191-198
-
-
Tien, H.F.1
Wang, C.H.2
Lee, F.U.3
Liu, M.C.4
Chuang, S.M.5
Chen, Y.C.6
Shen, M.C.7
Lin, D.T.8
Lin, K.H.9
Chu, W.M.10
|