122 related articles for article (PubMed ID: 17487754)
1. Loss of i(8)(q10) at relapse in two cases of childhood acute myeloid leukaemia.
Seppa L; Hengartner H; Leibundgut K; Kuhne T; Niggli FK; Betts DR
Leuk Lymphoma; 2007 May; 48(5):1045-7. PubMed ID: 17487754
[No Abstract] [Full Text] [Related]
2. Acute myeloid leukemia with a novel t(8;21) variant: paracentric inversion-associated ins(21;8).
Lee JH; Wan TS; Ha JS
Leuk Lymphoma; 2014 Feb; 55(2):441-3. PubMed ID: 23672346
[No Abstract] [Full Text] [Related]
3. A cryptic three-way translocation involving chromosomes 8, 14, and 21 in a case of acute myeloid leukemia subtype M1.
Lau LC; Koh LP; Lim TH; Loo LE; Tien SL
Cancer Genet Cytogenet; 2005 Nov; 163(1):86-90. PubMed ID: 16271963
[No Abstract] [Full Text] [Related]
4. Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2.
Hilgenfeld E; Padilla-Nash H; McNeil N; Knutsen T; Montagna C; Tchinda J; Horst J; Ludwig WD; Serve H; Büchner T; Berdel WE; Schröck E; Ried T
Br J Haematol; 2001 May; 113(2):305-17. PubMed ID: 11380393
[TBL] [Abstract][Full Text] [Related]
5. Translocation (8;21) in acute nonlymphocytic leukemia delineated by chromosomal in situ suppression hybridization.
Popp S; Jauch A; Qiu JY; Smialek B; Cremer T; Becher R
Cancer Genet Cytogenet; 1991 Nov; 57(1):103-7. PubMed ID: 1756476
[TBL] [Abstract][Full Text] [Related]
6. Late-appearing Philadelphia chromosome in childhood acute myeloid leukemia.
Shah N; Leaker MT; Teshima I; Baruchel S; Abdelhaleem M; Ye CC
Pediatr Blood Cancer; 2008 May; 50(5):1052-3. PubMed ID: 18213712
[TBL] [Abstract][Full Text] [Related]
7. Isochromosome (17)(q10) and translocation (4;12)(q12;p13) in a child with acute myeloid leukemia.
Nathan PC; Chun K; Abdelhaleem M; Malkin D
Cancer Genet Cytogenet; 2001 Nov; 131(1):82-5. PubMed ID: 11734325
[TBL] [Abstract][Full Text] [Related]
8. Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21).
Choi J; Song J; Kim SJ; Choi JR; Kim SJ; Min YH; Park TS; Cho SY; Kim MJ
Cancer Genet Cytogenet; 2010 Oct; 202(2):141-3. PubMed ID: 20875878
[No Abstract] [Full Text] [Related]
9. Acute myeloblastic leukemia associated with trisomy 8 and translocation 8;21 in a child with Down syndrome.
Yamaguchi Y; Fujii H; Kazama H; Iinuma K; Shinomiya N; Aoki T
Cancer Genet Cytogenet; 1997 Aug; 97(1):32-4. PubMed ID: 9242215
[TBL] [Abstract][Full Text] [Related]
10. Multiplex fluorescence in situ hybridization in identifying chromosome involvement of complex karyotypes in de novo myelodysplastic syndromes and acute myeloid leukemia.
Xu W; Li JY; Liu Q; Zhu Y; Pan JL; Qiu HR; Xue YQ
Int J Lab Hematol; 2010 Feb; 32(1 Pt 1):e86-95. PubMed ID: 20089000
[TBL] [Abstract][Full Text] [Related]
11. Clonal trisomy 11 in a child with acute leukemia: G banding vs. FISH.
Jadhav M; Cushing B; Ozdemir O; Mohamed A; Ravindranath Y; Savaşan S
Med Pediatr Oncol; 2001 Nov; 37(5):475-6. PubMed ID: 11745878
[No Abstract] [Full Text] [Related]
12. Detection of recurrent cytogenetic abnormalities in acute lymphoblastic and myeloid leukemias using fluorescence in situ hybridization.
Vance GH
Methods Mol Biol; 2013; 999():79-91. PubMed ID: 23666691
[TBL] [Abstract][Full Text] [Related]
13. Fifty-one patients with acute myeloid leukemia and translocation t(8;21)(q22;q22): an additional deletion in 9q is an adverse prognostic factor.
Schoch C; Haase D; Haferlach T; Gudat H; Büchner T; Freund M; Link H; Lengfelder E; Wandt H; Sauerland MC; Löffler H; Fonatsch C
Leukemia; 1996 Aug; 10(8):1288-95. PubMed ID: 8709633
[TBL] [Abstract][Full Text] [Related]
14. Acute myeloid leukaemia with variant t(8;21)(q22;q22) as a result of cryptic ins(8;21).
Wong KF; Siu LL
Pathology; 2011 Feb; 43(2):180-2. PubMed ID: 21233687
[No Abstract] [Full Text] [Related]
15. Chromosomal translocations in AML: detection and prognostic significance.
Palanisamy N
Cancer Treat Res; 2010; 145():41-58. PubMed ID: 20306244
[No Abstract] [Full Text] [Related]
16. Partial trisomy of chromosome 4 resulting from a novel t[4;7) translocation in a case of AML M2 with eosinophilia.
Hiorns LR; Swansbury GJ; Zomas A; Catovsky D
Cancer Genet Cytogenet; 1996 Jan; 86(1):89-91. PubMed ID: 8616799
[No Abstract] [Full Text] [Related]
17. Early blastic transformation of a myeloproliferative disorder with t(8;21) and progressive aberrations of chromosome 8.
Fasanaro A; Paone G; Silvestri I; Marottoli V; Cimino R; Ferrara F
Cancer Genet Cytogenet; 1994 Jul; 75(2):106-10. PubMed ID: 8055472
[TBL] [Abstract][Full Text] [Related]
18. Papular exanthem discloses acute myeloid leukaemia: interphase fluorescence in situ hybridization revealed deletion of p53 and gain at 8q22/8q24/Tel8q without trisomy 8.
Kaune KM; Baumgart M; Schmitke E; Haase D; Middel P; Ghadimi BM; Bertsch HP; Neumann C; Emmert S
Clin Exp Dermatol; 2010 Mar; 35(2):160-4. PubMed ID: 19438543
[TBL] [Abstract][Full Text] [Related]
19. Variant t(8;18;21) translocation in acute myeloid leukemia.
Uchida H; Ohyashiki K; Toyama K; Kondo M; Ito H; Ohsumi A
Cancer Genet Cytogenet; 1988 Dec; 36(2):231-2. PubMed ID: 3203317
[No Abstract] [Full Text] [Related]
20. Distinct clonal anomalies involving RUNX1 in acute myeloid leukemia at diagnosis and after bone marrow transplantation.
De Braekeleer E; Douet-Guilbert N; Basinko A; Le Bris MJ; Morel F; Berthou C; Férec C; De Braekeleer M
Ann Hematol; 2010 Dec; 89(12):1277-81. PubMed ID: 20352434
[No Abstract] [Full Text] [Related]
[Next] [New Search]
