-
1
-
-
0000638625
-
Simultaneous occurrence of mongolism and leukemia: Report of a nationwide survey
-
Krivit W, Good RA. Simultaneous occurrence of mongolism and leukemia: report of a nationwide survey. AMA J Dis Child. 1957;94:289-293.
-
(1957)
AMA J Dis Child
, vol.94
, pp. 289-293
-
-
Krivit, W.1
Good, R.A.2
-
2
-
-
0035412104
-
Pattern of malignant disorders in individuals with Down's syndrome
-
Hasle H. Pattern of malignant disorders in individuals with Down's syndrome. Lancet Oncol. 2001;2:429-436.
-
(2001)
Lancet Oncol
, vol.2
, pp. 429-436
-
-
Hasle, H.1
-
3
-
-
0023459992
-
Megakaryoblastic leukemia and Down's syndrome: A review
-
Zipursky A, Peeters M, Poon A. Megakaryoblastic leukemia and Down's syndrome: a review. Pediatr Hematol Oncol. 1987;4:211-230.
-
(1987)
Pediatr Hematol Oncol
, vol.4
, pp. 211-230
-
-
Zipursky, A.1
Peeters, M.2
Poon, A.3
-
4
-
-
0029838764
-
Myelodysplasia and acute myelogenous leukemia in Down's syndrome: A report of 40 children of the AML-BFM Study Group
-
Creutzig U, Ritter J, Vormoor J, et al. Myelodysplasia and acute myelogenous leukemia in Down's syndrome: a report of 40 children of the AML-BFM Study Group. Leukemia. 1996;10:1677-1686.
-
(1996)
Leukemia
, vol.10
, pp. 1677-1686
-
-
Creutzig, U.1
Ritter, J.2
Vormoor, J.3
-
5
-
-
0342905433
-
Risks of leukaemia and solid tumours in inviduals with Down's syndrome
-
Hasle H, Clemmensen IH, Mikkelsen M. Risks of leukaemia and solid tumours in inviduals with Down's syndrome. Lancet. 2000;355:165-169.
-
(2000)
Lancet
, vol.355
, pp. 165-169
-
-
Hasle, H.1
Clemmensen, I.H.2
Mikkelsen, M.3
-
7
-
-
33645240282
-
Perspective: Chromosomal aneuploidy in leukemia: lessons from down syndrome
-
Izraeli S. Perspective: chromosomal aneuploidy in leukemia: lessons from down syndrome. Hematol Oncol. 2006;24:3-6.
-
(2006)
Hematol Oncol
, vol.24
, pp. 3-6
-
-
Izraeli, S.1
-
8
-
-
0027276321
-
Immunophenotypes and karyotypes of leukemic cells in children with Down syndrome and acute lymphoblastic leukemia
-
Pui C-H, Raimondi SC, Borowitz MJ, et al. Immunophenotypes and karyotypes of leukemic cells in children with Down syndrome and acute lymphoblastic leukemia. J Clin Oncol. 1993;11:1361-1367.
-
(1993)
J Clin Oncol
, vol.11
, pp. 1361-1367
-
-
Pui, C.-H.1
Raimondi, S.C.2
Borowitz, M.J.3
-
9
-
-
0027420675
-
Trisomy 21 in childhood acute lymphoblastic leukemia: A Pediatric Oncology Group study (8602)
-
Watson MS, Carroll AJ, Shuster JJ, et al. Trisomy 21 in childhood acute lymphoblastic leukemia: a Pediatric Oncology Group study (8602). Blood. 1993;82:3098-3102.
-
(1993)
Blood
, vol.82
, pp. 3098-3102
-
-
Watson, M.S.1
Carroll, A.J.2
Shuster, J.J.3
-
10
-
-
0029153163
-
Acute leukemia and the transient myeloproliferative disorder associated with Down syndrome: Morphologic, immunophenotypic and cytogenetic manifestations
-
Litz CE, Davies S, Brunning RD, et al. Acute leukemia and the transient myeloproliferative disorder associated with Down syndrome: morphologic, immunophenotypic and cytogenetic manifestations. Leukemia. 1995;9:1432-1439.
-
(1995)
Leukemia
, vol.9
, pp. 1432-1439
-
-
Litz, C.E.1
Davies, S.2
Brunning, R.D.3
-
11
-
-
17344365412
-
Down's syndrome in childhood acute lymphoblastic leukemia: Clinical characteristics and treatment outcome in four consecutive BFM trials
-
Dördelmann M, Schrappe M, Reiter A, et al. Down's syndrome in childhood acute lymphoblastic leukemia: clinical characteristics and treatment outcome in four consecutive BFM trials. Leukemia. 1998;12:645-651.
-
(1998)
Leukemia
, vol.12
, pp. 645-651
-
-
Dördelmann, M.1
Schrappe, M.2
Reiter, A.3
-
12
-
-
0034809324
-
Down's syndrome and acute lymphoblastic leukaemia: Clinical features and response to treatment
-
Chessells JM, Harrison G, Richards SM, et al. Down's syndrome and acute lymphoblastic leukaemia: clinical features and response to treatment. Arch Dis Child. 2001;85:321-325.
-
(2001)
Arch Dis Child
, vol.85
, pp. 321-325
-
-
Chessells, J.M.1
Harrison, G.2
Richards, S.M.3
-
13
-
-
10044239576
-
Lymphoblast biology and outcome among children with Down syndrome and ALL treated on CCG-1952
-
Bassal M, La MK, Whitlock JA, et al. Lymphoblast biology and outcome among children with Down syndrome and ALL treated on CCG-1952. Pediatr Blood Cancer. 2005;44:21-28.
-
(2005)
Pediatr Blood Cancer
, vol.44
, pp. 21-28
-
-
Bassal, M.1
MK, L.2
Whitlock, J.A.3
-
14
-
-
28844446288
-
Clinical characteristics and outcome of children with Down syndrome and acute lymphoblastic leukemia: A Children's Cancer Group study
-
Whitlock JA, Sather HN, Gaynon P, et al. Clinical characteristics and outcome of children with Down syndrome and acute lymphoblastic leukemia: a Children's Cancer Group study. Blood. 2005;106:4043-4049.
-
(2005)
Blood
, vol.106
, pp. 4043-4049
-
-
Whitlock, J.A.1
Sather, H.N.2
Gaynon, P.3
-
15
-
-
20144388603
-
Acute leukaemia in children with Down syndrome: A population-based Nordic study
-
Zeller B, Gustafsson G, Forestier E, et al. Acute leukaemia in children with Down syndrome: a population-based Nordic study. Br J Haematol. 2005;128:797-804.
-
(2005)
Br J Haematol
, vol.128
, pp. 797-804
-
-
Zeller, B.1
Gustafsson, G.2
Forestier, E.3
-
16
-
-
0027362046
-
Two Down syndrome patients with an acquired translocation, t(8;14)(q11;q32), in early B-lineage acute lymphoblastic leukemia
-
Secker-Walker LM, Hawkins JM, Prentice HG, Mackie PH, Heerema NA, Provisor AJ. Two Down syndrome patients with an acquired translocation, t(8;14)(q11;q32), in early B-lineage acute lymphoblastic leukemia. Cancer Genet Cytogenet. 1993;70:148-150.
-
(1993)
Cancer Genet Cytogenet
, vol.70
, pp. 148-150
-
-
Secker-Walker, L.M.1
Hawkins, J.M.2
Prentice, H.G.3
Mackie, P.H.4
Heerema, N.A.5
Provisor, A.J.6
-
17
-
-
16144368041
-
Down syndrome, acute lymphoblastic leukemia, and t(8;14)(q11;q32)
-
Lee ACW, Chan LC, Kwong KW. Down syndrome, acute lymphoblastic leukemia, and t(8;14)(q11;q32). Cancer Genet Cytogenet. 1996;88:92.
-
(1996)
Cancer Genet Cytogenet
, vol.88
, pp. 92
-
-
Lee, A.C.W.1
Chan, L.C.2
Kwong, K.W.3
-
18
-
-
0004783768
-
Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries
-
Forestier E, Johansson B, Borgström G, Kerndrup G, Johannsson J, Heim S. Cytogenetic findings in a population-based series of 787 childhood acute lymphoblastic leukemias from the Nordic countries. Eur J Haematol. 2000;64:194-200.
-
(2000)
Eur J Haematol
, vol.64
, pp. 194-200
-
-
Forestier, E.1
Johansson, B.2
Borgström, G.3
Kerndrup, G.4
Johannsson, J.5
Heim, S.6
-
19
-
-
0033962655
-
Acute lymphoblastic leukemia with an unusual t(8;14)(q11.2;q32): A Pediatric Oncology Group study
-
Kaleem Z, Shuster JJ, Carroll AJ, et al. Acute lymphoblastic leukemia with an unusual t(8;14)(q11.2;q32): a Pediatric Oncology Group study. Leukemia. 2000;14:238-240.
-
(2000)
Leukemia
, vol.14
, pp. 238-240
-
-
Kaleem, Z.1
Shuster, J.J.2
Carroll, A.J.3
-
20
-
-
17944374922
-
Three further cases of t(8;14)(q11.2;q32) in acute lymphoblastic leukemia
-
Byatt S-A, Cheung K-L, Lillington DM, et al. Three further cases of t(8;14)(q11.2;q32) in acute lymphoblastic leukemia. Leukemia. 2001;15:1304-1305.
-
(2001)
Leukemia
, vol.15
, pp. 1304-1305
-
-
Byatt, S.-A.1
Cheung, K.-L.2
Lillington, D.M.3
-
21
-
-
0037308761
-
Acute lymphoblastic leukemia characterized by t(8;14)(q11.2;q32)
-
Moore S, Suttle J, Bain S, Story C, Rice M. Acute lymphoblastic leukemia characterized by t(8;14)(q11.2;q32). Cancer Genet Cytogenet. 2003;141:1-4.
-
(2003)
Cancer Genet Cytogenet
, vol.141
, pp. 1-4
-
-
Moore, S.1
Suttle, J.2
Bain, S.3
Story, C.4
Rice, M.5
-
22
-
-
16944363891
-
The common TEL/AML1 rearrangement does not represent a frequent event in acute lymphoblastic leukaemia occurring in children with Down syndrome
-
Lanza C, Volpe G, Basso G, et al. The common TEL/AML1 rearrangement does not represent a frequent event in acute lymphoblastic leukaemia occurring in children with Down syndrome. Leukemia. 1997;11:820-821.
-
(1997)
Leukemia
, vol.11
, pp. 820-821
-
-
Lanza, C.1
Volpe, G.2
Basso, G.3
-
23
-
-
0032907413
-
Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion
-
Loncarevic IF, Roitzheim B, Ritterbach J, et al. Trisomy 21 is a recurrent secondary aberration in childhood acute lymphoblastic leukemia with TEL/AML1 gene fusion. Genes Chromosomes Cancer. 1999;24:272-277.
-
(1999)
Genes Chromosomes Cancer
, vol.24
, pp. 272-277
-
-
Loncarevic, I.F.1
Roitzheim, B.2
Ritterbach, J.3
-
24
-
-
0034920241
-
Expression of TEL-AML1 fusion transcripts and response to induction therapy in standard risk acute lymphoblastic leukemia
-
Uckun FM, Pallisgaard N, Hokland P, et al. Expression of TEL-AML1 fusion transcripts and response to induction therapy in standard risk acute lymphoblastic leukemia. Leuk Lymphoma. 2001;42:41-56.
-
(2001)
Leuk Lymphoma
, vol.42
, pp. 41-56
-
-
Uckun, F.M.1
Pallisgaard, N.2
Hokland, P.3
-
25
-
-
18044369474
-
Equal frequency of TEL/AML1 rearrangements in children with acute lymphoblastic leukemia with and without Down syndrome
-
Steiner M, Attarbaschi A, König M, et al. Equal frequency of TEL/AML1 rearrangements in children with acute lymphoblastic leukemia with and without Down syndrome. Pediatr Hematol Oncol. 2005;22:229-234.
-
(2005)
Pediatr Hematol Oncol
, vol.22
, pp. 229-234
-
-
Steiner, M.1
Attarbaschi, A.2
König, M.3
-
26
-
-
0036727413
-
Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome
-
Wechsler J, Greene M, McDevitt MA, et al. Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndrome. Nat Genet. 2002;32:148-152.
-
(2002)
Nat Genet
, vol.32
, pp. 148-152
-
-
Wechsler, J.1
Greene, M.2
McDevitt, M.A.3
-
27
-
-
11144242549
-
Origins of leukaemia in children with Down syndrome
-
Hitzler JK, Zipursky A. Origins of leukaemia in children with Down syndrome. Nat Rev Cancer. 2005;5:11-20.
-
(2005)
Nat Rev Cancer
, vol.5
, pp. 11-20
-
-
Hitzler, J.K.1
Zipursky, A.2
-
28
-
-
0042243593
-
Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21
-
Rainis L, Bercovich D, Strehl S, et al. Mutations in exon 2 of GATA1 are early events in megakaryocytic malignancies associated with trisomy 21. Blood. 2003;102:981-986.
-
(2003)
Blood
, vol.102
, pp. 981-986
-
-
Rainis, L.1
Bercovich, D.2
Strehl, S.3
-
29
-
-
0021893601
-
Cytogenetic pattern in leukemic cells of patients with constitutional chromosome anomalies
-
Alimena G, Billström R, Casalone R, Gallo E, Mitelman F, Pasquali F. Cytogenetic pattern in leukemic cells of patients with constitutional chromosome anomalies. Cancer Genet Cytogenet. 1985;16:207-218.
-
(1985)
Cancer Genet Cytogenet
, vol.16
, pp. 207-218
-
-
Alimena, G.1
Billström, R.2
Casalone, R.3
Gallo, E.4
Mitelman, F.5
Pasquali, F.6
-
30
-
-
0025915835
-
The t(1;22)(p13;q13) is nonrandom and restricted to infants with acute megakaryoblastic leukemia: A Pediatric Oncology Group study
-
Carroll A, Civin C, Schneider N, et al. The t(1;22)(p13;q13) is nonrandom and restricted to infants with acute megakaryoblastic leukemia: a Pediatric Oncology Group study. Blood. 1991;78:748-752.
-
(1991)
Blood
, vol.78
, pp. 748-752
-
-
Carroll, A.1
Civin, C.2
Schneider, N.3
-
31
-
-
0026654207
-
The translocation t(1;22)(p13;q13) is a nonrandom marker specifically associated with acute megakaryocytic leukemia in young children
-
Lion T, Haas OA, Harbott J, et al. The translocation t(1;22)(p13;q13) is a nonrandom marker specifically associated with acute megakaryocytic leukemia in young children. Blood. 1992;79:3325-3330.
-
(1992)
Blood
, vol.79
, pp. 3325-3330
-
-
Lion, T.1
Haas, O.A.2
Harbott, J.3
-
32
-
-
0027300175
-
Review of the cytogenetic changes in acute megakaryoblastic leukemia: One disease or several?
-
Lu G, Altman AJ, Benn PA. Review of the cytogenetic changes in acute megakaryoblastic leukemia: one disease or several? Cancer Genet Cytogenet. 1993;67:81-89.
-
(1993)
Cancer Genet Cytogenet
, vol.67
, pp. 81-89
-
-
Lu, G.1
Altman, A.J.2
Benn, P.A.3
-
33
-
-
0028918255
-
Clinical and prognostic significance of chromosomal abnormalities in childhood acute myeloid leukemia de novo
-
Martinez-Climent JA, Lane NJ, Rubin CM, et al. Clinical and prognostic significance of chromosomal abnormalities in childhood acute myeloid leukemia de novo. Leukemia. 1995;9:95-101.
-
(1995)
Leukemia
, vol.9
, pp. 95-101
-
-
Martinez-Climent, J.A.1
Lane, N.J.2
Rubin, C.M.3
-
34
-
-
16744366910
-
Distinctive demography, biology, and outcome of acute myeloid leukemia and myelodysplastic syndrome in children with Down syndrome: Children's Cancer Group studies 2861 and 2891
-
Lange BJ, Kobrinsky N, Barnard DR, et al. Distinctive demography, biology, and outcome of acute myeloid leukemia and myelodysplastic syndrome in children with Down syndrome: Children's Cancer Group studies 2861 and 2891. Blood. 1998;91:608-615.
-
(1998)
Blood
, vol.91
, pp. 608-615
-
-
Lange, B.J.1
Kobrinsky, N.2
Barnard, D.R.3
-
35
-
-
0033959279
-
Nineteen cases of the t(1;22)(p13;q13) acute megakaryoblastic leukaemia of infants/children and a review of 39 cases: Report from a t(1;22) study group
-
Bernstein J, Dastugue N, Haas OA, et al. Nineteen cases of the t(1;22)(p13;q13) acute megakaryoblastic leukaemia of infants/children and a review of 39 cases: report from a t(1;22) study group. Leukemia. 2000;14:216-218.
-
(2000)
Leukemia
, vol.14
, pp. 216-218
-
-
Bernstein, J.1
Dastugue, N.2
Haas, O.A.3
-
36
-
-
0034661191
-
A t(1;22)(p13;q13) in four children with acute megakaryoblastic leukemia (M7), two with Down syndrome
-
Trejo RMA, Aguilera RP, Nieto S, Kofman S. A t(1;22)(p13;q13) in four children with acute megakaryoblastic leukemia (M7), two with Down syndrome. Cancer Genet Cytogenet. 2000;120:160-162.
-
(2000)
Cancer Genet Cytogenet
, vol.120
, pp. 160-162
-
-
Trejo, R.M.A.1
Aguilera, R.P.2
Nieto, S.3
Kofman, S.4
-
37
-
-
0037100420
-
Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): A study of the Groupe Français de Cytogéné tique Hématologique (GFCH)
-
Dastugue N, Lafage-Pochitaloff M, Pagès M-P, et al. Cytogenetic profile of childhood and adult megakaryoblastic leukemia (M7): a study of the Groupe Français de Cytogéné tique Hématologique (GFCH). Blood. 2002;100:618-626.
-
(2002)
Blood
, vol.100
, pp. 618-626
-
-
Dastugue, N.1
Lafage-Pochitaloff, M.2
Pagès, M.-P.3
-
38
-
-
0038730639
-
Cytogenetic abnormalities in childhood acute myeloid leukaemia: A Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001
-
Forestier E, Heim S, Blennow E, et al. Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001. Br J Haematol. 2003;121:566-577.
-
(2003)
Br J Haematol
, vol.121
, pp. 566-577
-
-
Forestier, E.1
Heim, S.2
Blennow, E.3
-
39
-
-
33644905562
-
Treatment for myeloid leukaemia of Down syndrome: Population-based experience in the UK and results from the Medical Research Council AML 10 and AML 12 trials
-
Rao A, Hills RK, Stiller C, et al. Treatment for myeloid leukaemia of Down syndrome: population-based experience in the UK and results from the Medical Research Council AML 10 and AML 12 trials. Br J Haematol. 2005;132:576-583.
-
(2005)
Br J Haematol
, vol.132
, pp. 576-583
-
-
Rao, A.1
Hills, R.K.2
Stiller, C.3
-
40
-
-
0019375797
-
Chromosome abnormalities in Down's syndrome patients with acute leukemia
-
Kaneko Y, Rowley JD, Variakojis D, Chilcote RR, Moohr JW, Patel D. Chromosome abnormalities in Down's syndrome patients with acute leukemia. Blood. 1981;58:459-466.
-
(1981)
Blood
, vol.58
, pp. 459-466
-
-
Kaneko, Y.1
Rowley, J.D.2
Variakojis, D.3
Chilcote, R.R.4
Moohr, J.W.5
Patel, D.6
-
41
-
-
0021991702
-
Acute leukemia characterized by trisomy 8 in Down's syndrome
-
Broomhead AF, Kwan YL, Zell NA, Lam-Po-Tang PRL, O'Gorman Hughes D. Acute leukemia characterized by trisomy 8 in Down's syndrome. Pathology. 1985;17:111-114.
-
(1985)
Pathology
, vol.17
, pp. 111-114
-
-
Broomhead, A.F.1
Kwan, Y.L.2
Zell, N.A.3
Lam-Po-Tang, P.R.L.4
O'Gorman Hughes, D.5
-
42
-
-
0023200439
-
Nonrandom chromosomal aberrations and clonal chromosomal evolution in acute leukemia associated with Down's syndrome
-
Wang N, Leung J, Warrier RP, et al. Nonrandom chromosomal aberrations and clonal chromosomal evolution in acute leukemia associated with Down's syndrome. Cancer Genet Cytogenet. 1987;28:155-162.
-
(1987)
Cancer Genet Cytogenet
, vol.28
, pp. 155-162
-
-
Wang, N.1
Leung, J.2
Warrier, R.P.3
-
43
-
-
0025131152
-
Leukaemia and transient leukaemia in Down syndrome
-
Iselius L, Jacobs P, Morton N. Leukaemia and transient leukaemia in Down syndrome. Hum Genet. 1990;85:477-485.
-
(1990)
Hum Genet
, vol.85
, pp. 477-485
-
-
Iselius, L.1
Jacobs, P.2
Morton, N.3
-
44
-
-
0025786573
-
Chromosome abnormalities and prognosis in childhood acute leukemia
-
Hayashi Y, Hanada R, Yamamoto K. Chromosome abnormalities and prognosis in childhood acute leukemia. Acta Paediatr Jpn. 1991;33:497-506.
-
(1991)
Acta Paediatr Jpn
, vol.33
, pp. 497-506
-
-
Hayashi, Y.1
Hanada, R.2
Yamamoto, K.3
-
45
-
-
0025923394
-
Chromosomenaberrationen bei akuten Leukämien im Kindesalter: Analyse von 1009 Patienten.
-
Lampert F, Harbott J, Ritterbach J. Chromosomenaberrationen bei akuten Leukämien im Kindesalter: Analyse von 1009 Patienten. Klin Pädiatr. 1991;203:311-318.
-
(1991)
Klin Pädiatr
, vol.203
, pp. 311-318
-
-
Lampert, F.1
Harbott, J.2
Ritterbach, J.3
-
46
-
-
0026808789
-
Acute myeloid leukemia (AML) in Down's syndrome is highly responsive to chemotherapy: Experience on Pediatric Oncology Group AML study 8498
-
Ravindranath Y, Abella E, Krischer JP, et al. Acute myeloid leukemia (AML) in Down's syndrome is highly responsive to chemotherapy: experience on Pediatric Oncology Group AML study 8498. Blood. 1992;80:2210-2214.
-
(1992)
Blood
, vol.80
, pp. 2210-2214
-
-
Ravindranath, Y.1
Abella, E.2
Krischer, J.P.3
-
47
-
-
0028213440
-
Myelodysplasia and acute megakaryoblastic leukemia in Down's syndrome
-
Zipursky A, Thorner P, De Harven E, Christensen H, Doyle J. Myelodysplasia and acute megakaryoblastic leukemia in Down's syndrome. Leuk Res. 1994;18:163-171.
-
(1994)
Leuk Res
, vol.18
, pp. 163-171
-
-
Zipursky, A.1
Thorner, P.2
De Harven, E.3
Christensen, H.4
Doyle, J.5
-
49
-
-
33947430093
-
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature
-
Forestier E, Andersen MK, Autio K, et al. Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: a Nordic series of 245 cases and review of the literature. Genes Chromosomes Cancer. 2007;46:440-450.
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 440-450
-
-
Forestier, E.1
Andersen, M.K.2
Autio, K.3
-
50
-
-
0030294909
-
Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes
-
Mertens F, Johansson B, Mitelman F. Dichotomy of hyperdiploid acute lymphoblastic leukemia on the basis of the distribution of gained chromosomes. Cancer Genet Cytogenet. 1996;92:8-10.
-
(1996)
Cancer Genet Cytogenet
, vol.92
, pp. 8-10
-
-
Mertens, F.1
Johansson, B.2
Mitelman, F.3
-
51
-
-
34249065493
-
Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia
-
Heerema NA, Raimondi SC, Anderson JR, et al. Specific extra chromosomes occur in a modal number dependent pattern in pediatric acute lymphoblastic leukemia. Genes Chromosomes Cancer. 2007;46:684-693.
-
(2007)
Genes Chromosomes Cancer
, vol.46
, pp. 684-693
-
-
Heerema, N.A.1
Raimondi, S.C.2
Anderson, J.R.3
-
52
-
-
0026748638
-
Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia
-
Onodera N, McCabe NR, Rubin CM. Formation of a hyperdiploid karyotype in childhood acute lymphoblastic leukemia. Blood. 1992;80:203-208.
-
(1992)
Blood
, vol.80
, pp. 203-208
-
-
Onodera, N.1
McCabe, N.R.2
Rubin, C.M.3
-
53
-
-
0141992996
-
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia
-
Paulsson K, Panagopoulos I, Knuutila S, et al. Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia. Blood. 2003;102:3010-3015.
-
(2003)
Blood
, vol.102
, pp. 3010-3015
-
-
Paulsson, K.1
Panagopoulos, I.2
Knuutila, S.3
-
54
-
-
24944520140
-
Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia
-
Paulsson K, Mörse H, Fioretos T, Behrendtz M, Strömbeck B, Johansson B. Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia. Genes Chromosomes Cancer. 2005;44:113-122.
-
(2005)
Genes Chromosomes Cancer
, vol.44
, pp. 113-122
-
-
Paulsson, K.1
Mörse, H.2
Fioretos, T.3
Behrendtz, M.4
Strömbeck, B.5
Johansson, B.6
-
55
-
-
33747468624
-
The incidence peaks of the childhood acute leukemias reflect specific cytogenetic aberrations
-
Forestier E, Schmiegelow K. The incidence peaks of the childhood acute leukemias reflect specific cytogenetic aberrations. J Pediatr Hematol Oncol. 2006;28:486-495.
-
(2006)
J Pediatr Hematol Oncol
, vol.28
, pp. 486-495
-
-
Forestier, E.1
Schmiegelow, K.2
-
56
-
-
0141634051
-
Origins of chromosome translocations in childhood leukaemia
-
Greaves MF, Wiemels J. Origins of chromosome translocations in childhood leukaemia. Nat Rev Cancer. 2003;3:1-11.
-
(2003)
Nat Rev Cancer
, vol.3
, pp. 1-11
-
-
Greaves, M.F.1
Wiemels, J.2
-
57
-
-
0031026450
-
Aetiology of acute leukaemia
-
Greaves MF. Aetiology of acute leukaemia. Lancet. 1997;349:344-349.
-
(1997)
Lancet
, vol.349
, pp. 344-349
-
-
Greaves, M.F.1
-
58
-
-
0025580086
-
Clinical and biological characteristics of acute lymphocytic leukemia in children with Down syndrome
-
Kalwinsky DK, Raimondi SC, Bunin NJ, et al. Clinical and biological characteristics of acute lymphocytic leukemia in children with Down syndrome. Am J Med Genet. 1990;7:267-271.
-
(1990)
Am J Med Genet
, vol.7
, pp. 267-271
-
-
Kalwinsky, D.K.1
Raimondi, S.C.2
Bunin, N.J.3
-
59
-
-
0031056793
-
The commonly deleted region at 9p21-22 in lymphoblastic leukemias spans at least 400 kb and includes p16 but not p15 or the IFN gene cluster
-
Aguiar RCT, Sill H, Goldman JM, Cross NCP. The commonly deleted region at 9p21-22 in lymphoblastic leukemias spans at least 400 kb and includes p16 but not p15 or the IFN gene cluster. Leukemia. 1997;11:233-238.
-
(1997)
Leukemia
, vol.11
, pp. 233-238
-
-
Aguiar, R.C.T.1
Sill, H.2
Goldman, J.M.3
Cross, N.C.P.4
-
60
-
-
34147224008
-
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
-
Mullighan CG, Goorha A, Radtke I, et al. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature. 2007;446:758-764.
-
(2007)
Nature
, vol.446
, pp. 758-764
-
-
Mullighan, C.G.1
Goorha, A.2
Radtke, I.3
-
61
-
-
34147161800
-
Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)
-
Akasaka T, Balasas T, Russell LJ, et al. Five members of the CEBP transcription factor family are targeted by recurrent IGH translocations in B-cell precursor acute lymphoblastic leukemia (BCP-ALL). Blood. 2007;109:3451-3461.
-
(2007)
Blood
, vol.109
, pp. 3451-3461
-
-
Akasaka, T.1
Balasas, T.2
Russell, L.J.3
-
62
-
-
0023682893
-
Cytogenetic findings and clinical features in acute leukemia and transient myeloproliferative disorder in Down's syndrome
-
Hayashi Y, Eguchi M, Sugita K, et al. Cytogenetic findings and clinical features in acute leukemia and transient myeloproliferative disorder in Down's syndrome. Blood. 1988;72:15-23.
-
(1988)
Blood
, vol.72
, pp. 15-23
-
-
Hayashi, Y.1
Eguchi, M.2
Sugita, K.3
-
63
-
-
0027378164
-
Cytogenetic deletion maps of hematologic neoplasms: Circumstantial evidence for tumor suppressor loci
-
Johansson B, Mertens F, Mitelman F. Cytogenetic deletion maps of hematologic neoplasms: circumstantial evidence for tumor suppressor loci. Genes Chromosomes Cancer. 1993;8:205-218.
-
(1993)
Genes Chromosomes Cancer
, vol.8
, pp. 205-218
-
-
Johansson, B.1
Mertens, F.2
Mitelman, F.3
-
64
-
-
0027367903
-
6q deletions define distinct clinico-pathologic subsets of non-Hodgkin's lymphoma
-
Offit K, Parsa NZ, Gaidano G, et al. 6q deletions define distinct clinico-pathologic subsets of non-Hodgkin's lymphoma. Blood. 1993;82:2157-2162.
-
(1993)
Blood
, vol.82
, pp. 2157-2162
-
-
Offit, K.1
Parsa, N.Z.2
Gaidano, G.3
-
65
-
-
3042526114
-
A fluorescence in situ hybridization map of 6q deletions in acute lymphocytic leukemia: Identification and analysis of a candidate tumor suppressor gene
-
Sinclair PB, Sorour A, Martineau M, et al. A fluorescence in situ hybridization map of 6q deletions in acute lymphocytic leukemia: identification and analysis of a candidate tumor suppressor gene. Cancer Res. 2004;64:4089-4098.
-
(2004)
Cancer Res
, vol.64
, pp. 4089-4098
-
-
Sinclair, P.B.1
Sorour, A.2
Martineau, M.3
-
66
-
-
33745820368
-
FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: Implications for formation and pathogenetic outcome of the idic(7)(p11.2)
-
Schaad K, Strömbeck B, Mandahl N, et al. FISH mapping of i(7q) in acute leukemias and myxoid liposarcoma reveals clustered breakpoints in 7p11.2: implications for formation and pathogenetic outcome of the idic(7)(p11.2). Cytogenet Genome Res. 2006;114:126-130.
-
(2006)
Cytogenet Genome Res
, vol.114
, pp. 126-130
-
-
Schaad, K.1
Strömbeck, B.2
Mandahl, N.3
-
67
-
-
33846853947
-
Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes
-
Paulsson K, Johansson B. Trisomy 8 as the sole chromosomal aberration in acute myeloid leukemia and myelodysplastic syndromes. Pathol Biol. 2007;55:37-48.
-
(2007)
Pathol Biol
, vol.55
, pp. 37-48
-
-
Paulsson, K.1
Johansson, B.2
-
68
-
-
0023200187
-
Down's syndrome and leukemia: Epidemiology, genetics, cytogenetics and mechanisms of leukemogenesis
-
Fong C, Brodeur GM. Down's syndrome and leukemia: epidemiology, genetics, cytogenetics and mechanisms of leukemogenesis. Cancer Genet Cytogenet. 1987;28:55-76.
-
(1987)
Cancer Genet Cytogenet
, vol.28
, pp. 55-76
-
-
Fong, C.1
Brodeur, G.M.2
-
69
-
-
0042489821
-
Acute myeloid leukaemia not otherwise categorised
-
Jaffe ES, Harris NL, Stein H, Vardiman JW, eds, Lyon, France: IARC Press;
-
Brunning RD, Matutes E, Flandrin G, et al. Acute myeloid leukaemia not otherwise categorised. In: Jaffe ES, Harris NL, Stein H, Vardiman JW, eds. World Health Organization classification of tumours; pathology and genetics of tumours of haematopoietic and lymphoid tissues. Lyon, France: IARC Press; 2001:91-105.
-
(2001)
World Health Organization classification of tumours; pathology and genetics of tumours of haematopoietic and lymphoid tissues
, pp. 91-105
-
-
Brunning, R.D.1
Matutes, E.2
Flandrin, G.3
|