-
1
-
-
0000286732
-
A minute chromosome in human granulocytic leukemia
-
Nowell PC, Hungerford DA. A minute chromosome in human granulocytic leukemia. Science 1960;132:1497.
-
(1960)
Science
, vol.132
, pp. 1497
-
-
Nowell, P.C.1
Hungerford, D.A.2
-
2
-
-
0015694748
-
A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining
-
Rowley JD. A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining [Letter]. Nature 1973; 243:290-3.
-
(1973)
Nature
, vol.243
, pp. 290-293
-
-
Rowley, J.D.1
-
4
-
-
0025091057
-
Philadelphia chromosome positive childhood acute lymphoblastic leukemia: Clinical and cytogenetic characteristics and treatment outcome. A Pediatric Oncology Group study
-
Crist W, Carroll A, Shuster J, et al. Philadelphia chromosome positive childhood acute lymphoblastic leukemia: clinical and cytogenetic characteristics and treatment outcome. A Pediatric Oncology Group study. Blood 1990;76:489-94.
-
(1990)
Blood
, vol.76
, pp. 489-494
-
-
Crist, W.1
Carroll, A.2
Shuster, J.3
-
6
-
-
0027412262
-
Collaborative study of karyotypes in childhood acute lymphoblastic leukemias
-
GFCH: Groupe Francais de Cytogenetique Hematologique. Collaborative study of karyotypes in childhood acute lymphoblastic leukemias. Leukemia 1993;7:10-19.
-
(1993)
Leukemia
, vol.7
, pp. 10-19
-
-
-
7
-
-
0031034526
-
Cytogenetics adds independent prognostic information in adults with acute lymphoblastic leukaemia on MRC trial UKALL XA
-
Secker-Walker LM, Prentice HG, Durrant J, et al. Cytogenetics adds independent prognostic information in adults with acute lymphoblastic leukaemia on MRC trial UKALL XA. Br J Haematol 1997;96:601-10.
-
(1997)
Br J Haematol
, vol.96
, pp. 601-610
-
-
Secker-Walker, L.M.1
Prentice, H.G.2
Durrant, J.3
-
8
-
-
0028212488
-
Adult Philadelphia-chromosome-positive acute lymphoblastic leukemia: Experience of treatments during a ten-year period
-
Annino L, Ferrari A, Cedrone M, et al. Adult Philadelphia-chromosome-positive acute lymphoblastic leukemia: experience of treatments during a ten-year period. Leukemia 1994;8:664-7.
-
(1994)
Leukemia
, vol.8
, pp. 664-667
-
-
Annino, L.1
Ferrari, A.2
Cedrone, M.3
-
9
-
-
0017622954
-
The Philadelphia chromosome (Ph1) in adults presenting with acute leukaemia: A comparison of Ph1+ and Ph1 - Patients
-
Bloomfield CD, Peterson LC, Yunis JJ, et al. The Philadelphia chromosome (Ph1) in adults presenting with acute leukaemia: a comparison of Ph1+ and Ph1 - patients. Br J Haematol 1977;36:347-58.
-
(1977)
Br J Haematol
, vol.36
, pp. 347-358
-
-
Bloomfield, C.D.1
Peterson, L.C.2
Yunis, J.J.3
-
10
-
-
0025221547
-
Detection of bcr-abl fusion in chronic myelogeneous leukemia by in situ hybridization
-
Tkachuk DC, Westbrook CA, Andreeff M, et al. Detection of bcr-abl fusion in chronic myelogeneous leukemia by in situ hybridization. Science 1990;250:559-62.
-
(1990)
Science
, vol.250
, pp. 559-562
-
-
Tkachuk, D.C.1
Westbrook, C.A.2
Andreeff, M.3
-
11
-
-
0025601717
-
Molecular methods to detect the Philadelphia chromosome
-
Hooberman AL, Westbrook CA. Molecular methods to detect the Philadelphia chromosome. Clin Lab Med 1990;10:839-55.
-
(1990)
Clin Lab Med
, vol.10
, pp. 839-855
-
-
Hooberman, A.L.1
Westbrook, C.A.2
-
12
-
-
0015694741
-
Identification of a translocation with quinacrine fluorescence in a patient with acute leukemia
-
Rowley JD. Identification of a translocation with quinacrine fluorescence in a patient with acute leukemia. Ann Genet 1973;16:109-12.
-
(1973)
Ann Genet
, vol.16
, pp. 109-112
-
-
Rowley, J.D.1
-
13
-
-
0017162163
-
Proposals for the classification of the acute leukaemias
-
French-American-British (FAB) co-operative group
-
Bennett JM, Catovsky D, Daniel MT, et al. Proposals for the classification of the acute leukaemias. French-American-British (FAB) co-operative group. Br J Haematol 1976;33:451-8.
-
(1976)
Br J Haematol
, vol.33
, pp. 451-458
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.T.3
-
14
-
-
0022135739
-
Proposed revised criteria for the classification of acute myeloid leukemia
-
Bennett JM, Catovsky D, Daniel M, et al. Proposed revised criteria for the classification of acute myeloid leukemia. Ann Intern Med 1985;103:626-9.
-
(1985)
Ann Intern Med
, vol.103
, pp. 626-629
-
-
Bennett, J.M.1
Catovsky, D.2
Daniel, M.3
-
15
-
-
0027218725
-
The t(8;21) translocation in acute myeloid leukemia results in production of an AML1-MTG8 fusion transcript
-
Miyoshi H, Kozu T, Shimizu K, et al. The t(8;21) translocation in acute myeloid leukemia results in production of an AML1-MTG8 fusion transcript. EMBO J 1993;12:2715-21.
-
(1993)
EMBO J
, vol.12
, pp. 2715-2721
-
-
Miyoshi, H.1
Kozu, T.2
Shimizu, K.3
-
16
-
-
0028908542
-
Interphase cytogenetics of the t(8;21)(q22;q22) associated with acute myelogenous leukemia by two-color fluorescence in situ hybridization
-
Sacchi N, Magnani I, Kearney L, et al. Interphase cytogenetics of the t(8;21)(q22;q22) associated with acute myelogenous leukemia by two-color fluorescence in situ hybridization. Cancer Genet Cytogenet 1995;79:97-103.
-
(1995)
Cancer Genet Cytogenet
, vol.79
, pp. 97-103
-
-
Sacchi, N.1
Magnani, I.2
Kearney, L.3
-
17
-
-
26844486401
-
FISH analysis of masked t(8;21)(q22;q22) translocations
-
Harrison CJ, Ross F, Radford-Weiss I, et al. FISH analysis of masked t(8;21)(q22;q22) translocations. Br J Haematol 1996;93:238.
-
(1996)
Br J Haematol
, vol.93
, pp. 238
-
-
Harrison, C.J.1
Ross, F.2
Radford-Weiss, I.3
-
18
-
-
0017362792
-
15/17 translocation: A consistent chromosomal changek in acute promyelocytic leukaemia
-
Rowley JD, Golomb HM, Dougherty C. 15/17 translocation: a consistent chromosomal changek in acute promyelocytic leukaemia. Lancet 1977;i:549-50.
-
(1977)
Lancet
, vol.1
, pp. 549-550
-
-
Rowley, J.D.1
Golomb, H.M.2
Dougherty, C.3
-
19
-
-
0027957296
-
Acute promyelocytic leukemia: From genetics to treatment
-
Grignani F, Fagioli M, Alcalay M, et al. Acute promyelocytic leukemia: from genetics to treatment. Blood 1994;83:10-25.
-
(1994)
Blood
, vol.83
, pp. 10-25
-
-
Grignani, F.1
Fagioli, M.2
Alcalay, M.3
-
20
-
-
0028848626
-
Combined cytogenetic, FISH and molecular analysis in acute promyelocytic leukaemia at diagnosis and in complete remission
-
Mancini M, Nanni M, Cedrone M. Combined cytogenetic, FISH and molecular analysis in acute promyelocytic leukaemia at diagnosis and in complete remission. Br J Haematol 1995;91:878-84.
-
(1995)
Br J Haematol
, vol.91
, pp. 878-884
-
-
Mancini, M.1
Nanni, M.2
Cedrone, M.3
-
21
-
-
0020550724
-
Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia. A unique cytogenetic-clinicopathological association
-
Le Beau MM, Larson RA, Bitter MA, et al. Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia. A unique cytogenetic-clinicopathological association. N Engl J Med 1983;309:630-6.
-
(1983)
N Engl J Med
, vol.309
, pp. 630-636
-
-
Le Beau, M.M.1
Larson, R.A.2
Bitter, M.A.3
-
22
-
-
0027373893
-
Fusion between transcription factor CBF beta/PEBP beta and a myosin heavy chain in acute myeloid leukemia
-
Liu P, Tarle SS, Hajra A, et al. Fusion between transcription factor CBF beta/PEBP beta and a myosin heavy chain in acute myeloid leukemia. Science 1993;261:1041-44.
-
(1993)
Science
, vol.261
, pp. 1041-1044
-
-
Liu, P.1
Tarle, S.S.2
Hajra, A.3
-
23
-
-
0027304591
-
Identification of yeast artificial chromosomes containing the inversion 16 p-arm breakpoint associated with acute myelomemocytic leukemia
-
Liu P, Claxton DF, Marlton P, et al. Identification of yeast artificial chromosomes containing the inversion 16 p-arm breakpoint associated with acute myelomemocytic leukemia. Blood 1993;82:716-21.
-
(1993)
Blood
, vol.82
, pp. 716-721
-
-
Liu, P.1
Claxton, D.F.2
Marlton, P.3
-
24
-
-
0028330771
-
t(12;21): A new recurrent translocation in acute lymphoblastic leukemia
-
Romana SP, Le Coniat M, Berger R. t(12;21): a new recurrent translocation in acute lymphoblastic leukemia. Genes Chromosomes Cancer 1994;9:186-91.
-
(1994)
Genes Chromosomes Cancer
, vol.9
, pp. 186-191
-
-
Romana, S.P.1
Le Coniat, M.2
Berger, R.3
-
25
-
-
0029045087
-
The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion
-
Romana SP, Mauchauffe M, Le Coniat M, et al. The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion. Blood 1995;85:3662-70.
-
(1995)
Blood
, vol.85
, pp. 3662-3670
-
-
Romana, S.P.1
Mauchauffe, M.2
Le Coniat, M.3
-
26
-
-
0028805405
-
High frequently of t(12;21) in childhood B-lineage acute lymphoblastic leukemia
-
Romana SP, Poirel H, Leconiat M, et al. High frequently of t(12;21) in childhood B-lineage acute lymphoblastic leukemia. Blood 1995;86:4263-9.
-
(1995)
Blood
, vol.86
, pp. 4263-4269
-
-
Romana, S.P.1
Poirel, H.2
Leconiat, M.3
-
27
-
-
0028266479
-
Cytogenetic features of infants less than 12 months of age at diagnosis of acute lymphoblastic leukemia: Impact of the 11q23 breakpoint on outcome: a report of the Children's Cancer Group
-
Heerema NA, Arthur DC, Sather H, et al. Cytogenetic features of infants less than 12 months of age at diagnosis of acute lymphoblastic leukemia: impact of the 11q23 breakpoint on outcome: a report of the Children's Cancer Group. Blood 1994;83:2274-84.
-
(1994)
Blood
, vol.83
, pp. 2274-2284
-
-
Heerema, N.A.1
Arthur, D.C.2
Sather, H.3
-
28
-
-
0029018546
-
Molecular basis of 11q23 rearrangements in hematopoietic malignant proliferations
-
Bernard OA, Berger R. Molecular basis of 11q23 rearrangements in hematopoietic malignant proliferations. Genes Chromosomes Cancer 1995;13:75-85.
-
(1995)
Genes Chromosomes Cancer
, vol.13
, pp. 75-85
-
-
Bernard, O.A.1
Berger, R.2
-
29
-
-
0026767169
-
Acute leukemias with the t(4:11)(q21;q23)
-
Pui C. Acute leukemias with the t(4:11)(q21;q23). Leuk Lymphoma 1992;7:173-9.
-
(1992)
Leuk Lymphoma
, vol.7
, pp. 173-179
-
-
Pui, C.1
-
31
-
-
0022617302
-
Clinical and cytogenetic correlation in 63 patients with therapy-related myelodysplastic syndrome and acute non-lymphocytic leukemia: Further evidence of characteristic abnormalities of chromosomes 5 and 7
-
le Beau M, Albain KS, Larson RA, et al. Clinical and cytogenetic correlation in 63 patients with therapy-related myelodysplastic syndrome and acute non-lymphocytic leukemia: further evidence of characteristic abnormalities of chromosomes 5 and 7. J Clin Oncol 1986;4:325-45.
-
(1986)
J Clin Oncol
, vol.4
, pp. 325-345
-
-
Le Beau, M.1
Albain, K.S.2
Larson, R.A.3
-
32
-
-
0025019583
-
Detection of numerical chromosomal abnormalities in neoplastic hematopoietic cells by in situ hybridization with a chromosome-specific probe
-
Anastasi J, Le Beau MM, Vardiman JW, et al. Detection of numerical chromosomal abnormalities in neoplastic hematopoietic cells by in situ hybridization with a chromosome-specific probe. Am J Pathol 1990;136:131-9.
-
(1990)
Am J Pathol
, vol.136
, pp. 131-139
-
-
Anastasi, J.1
Le Beau, M.M.2
Vardiman, J.W.3
-
33
-
-
0027991276
-
Common region of deletion on the long arm of chromosome 6 in non-Hodgkin's lymphoma and acute lymphoblastic leukemia
-
Menasce LP, Orphanos V, Santibanez-Koref M, et al. Common region of deletion on the long arm of chromosome 6 in non-Hodgkin's lymphoma and acute lymphoblastic leukemia. Genes Chromosomes Cancer 1994;10:286-8.
-
(1994)
Genes Chromosomes Cancer
, vol.10
, pp. 286-288
-
-
Menasce, L.P.1
Orphanos, V.2
Santibanez-Koref, M.3
-
34
-
-
26844527237
-
Deletion of a common region on the long arm of chromosome 6 in acute lymphoblastic leukaemia
-
Menasce LP, Orphanos V, Santibanez-Koref M, et al. Deletion of a common region on the long arm of chromosome 6 in acute lymphoblastic leukaemia. Genes Chromosomes Cancer 1994;86:867-9.
-
(1994)
Genes Chromosomes Cancer
, vol.86
, pp. 867-869
-
-
Menasce, L.P.1
Orphanos, V.2
Santibanez-Koref, M.3
-
35
-
-
0030894471
-
Analysis of chromosome 6 deletions in lymphoid malignancies provides evidence for a minimal region of deletion within a 2-megabase segment of 6q21
-
Sherratt T, Morelli C, Boyle JM, Analysis of chromosome 6 deletions in lymphoid malignancies provides evidence for a minimal region of deletion within a 2-megabase segment of 6q21. Chromosome Res 1997,5:118-24.
-
(1997)
Chromosome Res
, vol.5
, pp. 118-124
-
-
Sherratt, T.1
Morelli, C.2
Boyle, J.M.3
-
36
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallioniemi A, Kalhoniemi O, Sudar D, et al. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 1992;258:818-21.
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kalhoniemi, O.2
Sudar, D.3
-
37
-
-
0027966172
-
Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumours
-
Kallioniemi O, Kallioniemi A, Piper J, et al. Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumours. Genes Chromosomes Cancer 1994;10:231-43.
-
(1994)
Genes Chromosomes Cancer
, vol.10
, pp. 231-243
-
-
Kallioniemi, O.1
Kallioniemi, A.2
Piper, J.3
-
38
-
-
0038214755
-
Multicolor spectral karyotyping of human chromosomes
-
Schrock E, du Manoir S, Veldman T, et al. Multicolor spectral karyotyping of human chromosomes. Science 1996;273:494-7.
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schrock, E.1
Du Manoir, S.2
Veldman, T.3
-
39
-
-
0029912473
-
Karyotyping human chromosomes by combinatorial multi-fluor FISH
-
Speicher MR, Ballard SG, Ward DC. Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nature Genet 1996;12:368-75.
-
(1996)
Nature Genet
, vol.12
, pp. 368-375
-
-
Speicher, M.R.1
Ballard, S.G.2
Ward, D.C.3
-
40
-
-
0030909689
-
Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral kayotyping
-
Veldman T, Vignon C, Schrock E, et al. Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral kayotyping. Nature Genet 1997;15:406-10.
-
(1997)
Nature Genet
, vol.15
, pp. 406-410
-
-
Veldman, T.1
Vignon, C.2
Schrock, E.3
-
41
-
-
0030974970
-
Increasing sensitivity of minimal residual disease detection by interphase FISH in acute lymphoblastic leukemia with hyperdiploidy
-
Kasprzyk A, Seeker-Walker LM. Increasing sensitivity of minimal residual disease detection by interphase FISH in acute lymphoblastic leukemia with hyperdiploidy. Leukemia 1997;11:429-35.
-
(1997)
Leukemia
, vol.11
, pp. 429-435
-
-
Kasprzyk, A.1
Seeker-Walker, L.M.2
-
42
-
-
0028905531
-
Detection of minimal residual disease in acute leukemia: Methodologic advances and clinical significance
-
Campana D, Pui C. Detection of minimal residual disease in acute leukemia: methodologic advances and clinical significance. Blood 1995;85:1416-34.
-
(1995)
Blood
, vol.85
, pp. 1416-1434
-
-
Campana, D.1
Pui, C.2
-
43
-
-
0021366234
-
Cytogenetic studies on recipients of allogeneic bone marrow using the sex chromosomes as markers of cellular origin
-
Lawler SD, Baker MC, Harris H, et al. Cytogenetic studies on recipients of allogeneic bone marrow using the sex chromosomes as markers of cellular origin. Br J Haematol 1984;56:431-43.
-
(1984)
Br J Haematol
, vol.56
, pp. 431-443
-
-
Lawler, S.D.1
Baker, M.C.2
Harris, H.3
-
44
-
-
0026023565
-
Intel-phase cytogenetic analysis detects minimal residual disease in a case of acute lymphoblastic leukemia and resolves the question of origin of relapse after allogeneic bone marrow transplantation
-
Anastasi J, Thangavelu M, Vardiman JW, et al. Intel-phase cytogenetic analysis detects minimal residual disease in a case of acute lymphoblastic leukemia and resolves the question of origin of relapse after allogeneic bone marrow transplantation. Blood 1991;77:1087-91.
-
(1991)
Blood
, vol.77
, pp. 1087-1091
-
-
Anastasi, J.1
Thangavelu, M.2
Vardiman, J.W.3
-
45
-
-
0025187739
-
Prognostic and biological importance of chromosome findings in acute lymphoblastic leukemia [10th anniversary article]
-
Secker-Walker LM. Prognostic and biological importance of chromosome findings in acute lymphoblastic leukemia [10th anniversary article]. Cancer Genet Cytogenet 1990:49:1-13.
-
(1990)
Cancer Genet Cytogenet
, vol.49
, pp. 1-13
-
-
Secker-Walker, L.M.1
-
46
-
-
0018088896
-
Prognostic implications of chromosomal findings in acute lymphoblastic leukaemia at diagnosis
-
Seeker-Walker LM, Lawler SD, Hardisty EM. Prognostic implications of chromosomal findings in acute lymphoblastic leukaemia at diagnosis. Br Med J 1978;2:1529-30.
-
(1978)
Br Med J
, vol.2
, pp. 1529-1530
-
-
Seeker-Walker, L.M.1
Lawler, S.D.2
Hardisty, E.M.3
-
47
-
-
0022653272
-
Chromosomal abnormalities identify high-risk and low-risk patients with acute lymphoblastic leukemia
-
Bloomfleld CD, Goldman AI, Alimena G, et al. Chromosomal abnormalities identify high-risk and low-risk patients with acute lymphoblastic leukemia. Blood 1986;67:415-20.
-
(1986)
Blood
, vol.67
, pp. 415-420
-
-
Bloomfleld, C.D.1
Goldman, A.I.2
Alimena, G.3
-
48
-
-
0028349911
-
11q23/MLL rearrangements confers a poor prognosis in infants with acute lymphoblastic leukemia
-
Pui CH, Behm FG, Downing JR, et al. 11q23/MLL rearrangements confers a poor prognosis in infants with acute lymphoblastic leukemia. J Clin Oncol 1994;12:909-15.
-
(1994)
J Clin Oncol
, vol.12
, pp. 909-915
-
-
Pui, C.H.1
Behm, F.G.2
Downing, J.R.3
-
49
-
-
0026094623
-
Near haploid acute lymphoblastic leukemia: Seven new cases and a review of the literature
-
Gibbons B, MacCallum P, Watts E, et al. Near haploid acute lymphoblastic leukemia: seven new cases and a review of the literature. Leukemia 1991;5:738-43.
-
(1991)
Leukemia
, vol.5
, pp. 738-743
-
-
Gibbons, B.1
MacCallum, P.2
Watts, E.3
-
50
-
-
0020299111
-
Cytogenetic studies on Burkitt's lymphoma-leukemia
-
Berger R, Bernheim A. Cytogenetic studies on Burkitt's lymphoma-leukemia. Cancer Genet Cytogenet 1982;7:231-44.
-
(1982)
Cancer Genet Cytogenet
, vol.7
, pp. 231-244
-
-
Berger, R.1
Bernheim, A.2
-
51
-
-
13344285351
-
Improved outcome in adult B-cell acute lymphoblastic leukemia
-
Hoelzer D, Ludwig W, Eckhard E, et al. Improved outcome in adult B-cell acute lymphoblastic leukemia. Blood 1996;87:495-508.
-
(1996)
Blood
, vol.87
, pp. 495-508
-
-
Hoelzer, D.1
Ludwig, W.2
Eckhard, E.3
-
52
-
-
0021330533
-
New chromosomal translocations correlate with specific immunophenotypes of childhood acute lymphoblastic leukemia
-
Williams DL, Look AT, Melvin SL, et al. New chromosomal translocations correlate with specific immunophenotypes of childhood acute lymphoblastic leukemia. Cell 1984;36:101-9.
-
(1984)
Cell
, vol.36
, pp. 101-109
-
-
Williams, D.L.1
Look, A.T.2
Melvin, S.L.3
-
53
-
-
26844497005
-
Clinical significance of the t(1;19)(q23;p13) in childhood acute lymphoblastic leukemia
-
Raimondi S, Roberson P, Behm FG, et al. Clinical significance of the t(1;19)(q23;p13) in childhood acute lymphoblastic leukemia [abstract]. Proc Am Assoc Cancer Res 1990;31:26.
-
(1990)
Proc Am Assoc Cancer Res
, vol.31
, pp. 26
-
-
Raimondi, S.1
Roberson, P.2
Behm, F.G.3
-
54
-
-
0026716252
-
Prognostic significance of the balanced t(1;19) and unbalanced der(19)t(1;19) translocations in acute lymphoblastic leukemia
-
Secker-Walker LM, Berger R, Fenaux P, et al. Prognostic significance of the balanced t(1;19) and unbalanced der(19)t(1;19) translocations in acute lymphoblastic leukemia. Leukemia 1992;6:363-9.
-
(1992)
Leukemia
, vol.6
, pp. 363-369
-
-
Secker-Walker, L.M.1
Berger, R.2
Fenaux, P.3
|