165 related articles for article (PubMed ID: 14999936)
1. [FISH detected 11q23 microdeletion and translocation at the long arm of chromosome 11 in a child with normal karyotypic acute lymphoblastic leukemia].
Matsubara K; Yura K
Rinsho Ketsueki; 2004 Jan; 45(1):61-5. PubMed ID: 14999936
[TBL] [Abstract][Full Text] [Related]
2. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
3. A case of infantile acute lymphoblastic leukemia presenting with rearrangement of MLL at 11q23 and apparent insertion or translocation at 10p12.
Tirado CA; Lager J; Rosoff PM; Golembiski-Ruiz V; Gong JZ; Goodman BK
Cancer Genet Cytogenet; 2004 Oct; 154(1):57-9. PubMed ID: 15381373
[TBL] [Abstract][Full Text] [Related]
4. Cytogenetic study of a patient with infant acute lymphoblastic leukemia using GTG-banding and chromosome painting.
Alter D; Mark HF
Exp Mol Pathol; 2000 Oct; 69(2):152-8. PubMed ID: 11001863
[TBL] [Abstract][Full Text] [Related]
5. Mixed lineage leukemia-rearranged childhood pro-B and CD10-negative pre-B acute lymphoblastic leukemia constitute a distinct clinical entity.
Attarbaschi A; Mann G; König M; Steiner M; Strehl S; Schreiberhuber A; Schneider B; Meyer C; Marschalek R; Borkhardt A; Pickl WF; Lion T; Gadner H; Haas OA; Dworzak MN
Clin Cancer Res; 2006 May; 12(10):2988-94. PubMed ID: 16707593
[TBL] [Abstract][Full Text] [Related]
6. [Cytogenetics and clinical studies of hematologic malignancies with 11q23 abnormalities in China].
Guo Y; Xue Y; Xie X; Wu D; Li J; Lu D; Jiang F; Geng M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Apr; 17(2):72-5. PubMed ID: 10751523
[TBL] [Abstract][Full Text] [Related]
7. Infant acute lymphoblastic leukemia - combined cytogenetic, immunophenotypical and molecular analysis of 77 cases.
Borkhardt A; Wuchter C; Viehmann S; Pils S; Teigler-Schlegel A; Stanulla M; Zimmermann M; Ludwig WD; Janka-Schaub G; Schrappe M; Harbott J
Leukemia; 2002 Sep; 16(9):1685-90. PubMed ID: 12200682
[TBL] [Abstract][Full Text] [Related]
8. [Establishment and application of multiplex FISH in detection of the complex chromosome abnormalities in leukemia].
Zhao M; Chen B; Wang L; Xu L; Cao Q; Su X; Chen S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Oct; 19(5):375-8. PubMed ID: 12362309
[TBL] [Abstract][Full Text] [Related]
9. Structure and significance of cytogenetic abnormalities in adult patients with Ph-negative acute lymphoblastic leukemia.
Piskunova IS; Obukhova TN; Parovichnikova EN; Kulikov SM; Troitskaya VV; Gavrilina OA; Savchenko VG
Ter Arkh; 2018 Aug; 90(7):30-37. PubMed ID: 30701920
[TBL] [Abstract][Full Text] [Related]
10. [Rearrangements of the mixed lineage leukemia gene in acute myeloid leukemia].
Zhang LJ; Lu XL; He J; Li Y
Zhonghua Yi Xue Za Zhi; 2006 Aug; 86(32):2256-60. PubMed ID: 17064570
[TBL] [Abstract][Full Text] [Related]
11. Identification of three distinct regions of deletion on the long arm of chromosome 11 in childhood acute lymphoblastic leukemia.
Takeuchi S; Cho SK; Seriu T; Koike M; Bartram CR; Reiter A; Schrappe M; Takeuchi C; Taguchi H; Koeffler HP
Oncogene; 1999 Dec; 18(51):7387-8. PubMed ID: 10602495
[TBL] [Abstract][Full Text] [Related]
12. The application of conventional cytogenetics, FISH, and RT-PCR to detect genetic changes in 70 children with ALL.
Soszynska K; Mucha B; Debski R; Skonieczka K; Duszenko E; Koltan A; Wysocki M; Haus O
Ann Hematol; 2008 Dec; 87(12):991-1002. PubMed ID: 18633615
[TBL] [Abstract][Full Text] [Related]
13. [Clinical significance and frequency of the 11q23/MLL genetic molecular alteration in Chilean infants with acute leukemia].
Cabrera ME; Campbell M; Quintana J; Undurraga MS; Ford AA; Greaves MF
Rev Med Chil; 2001 Jun; 129(6):634-42. PubMed ID: 11510203
[TBL] [Abstract][Full Text] [Related]
14. High frequency of t(12;21)(p13;q22) in children with acute lymphoblastic leukemia and known clinical outcome in southern Brazil.
Veiga LB; Cóser VM; Cavalli LR; Cavalli IJ; Rodrigues JN; Pereira WV; Pereira DV; Lafayette TC; Villalba BT; Moreira ME; Haddad BR; de Souza Fonseca Ribeiro EM
Leuk Res; 2004 Oct; 28(10):1033-8. PubMed ID: 15289014
[TBL] [Abstract][Full Text] [Related]
15. Clinical and molecular cytogenetic characteristics of dic(9;20) in adult acute lymphoblastic leukemia: a case report of three patients.
Song X; Gong S; Yang J; Wang J
Ann Hematol; 2007 May; 86(5):347-51. PubMed ID: 17245591
[TBL] [Abstract][Full Text] [Related]
16. Minimal residual disease values discriminate between low and high relapse risk in children with B-cell precursor acute lymphoblastic leukemia and an intrachromosomal amplification of chromosome 21: the Austrian and German acute lymphoblastic leukemia Berlin-Frankfurt-Munster (ALL-BFM) trials.
Attarbaschi A; Mann G; Panzer-Grümayer R; Röttgers S; Steiner M; König M; Csinady E; Dworzak MN; Seidel M; Janousek D; Möricke A; Reichelt C; Harbott J; Schrappe M; Gadner H; Haas OA
J Clin Oncol; 2008 Jun; 26(18):3046-50. PubMed ID: 18565891
[TBL] [Abstract][Full Text] [Related]
17. Diagnostic value of fluorescence in situ hybridization for the detection of genomic aberrations in older patients with acute myeloid leukemia.
Fröhling S; Kayser S; Mayer C; Miller S; Wieland C; Skelin S; Schlenk RF; Döhner H; Döhner K;
Haematologica; 2005 Feb; 90(2):194-9. PubMed ID: 15710571
[TBL] [Abstract][Full Text] [Related]
18. Acute lymphoblastic leukemia with 4;11 translocation analyzed by a multi-modal strategy of conventional cytogenetics, FISH, morphology, flow cytometry and molecular genetics, and review of the literature.
Hayne CC; Winer E; Williams T; Chaves F; Khorsand J; Mark HF
Exp Mol Pathol; 2006 Aug; 81(1):62-71. PubMed ID: 16765346
[TBL] [Abstract][Full Text] [Related]
19. [Detection of aberrant chromosomes in acute lymphoblastic leukemia by fluorescence in situ hybridization].
Yang K; Huang L
Zhonghua Xue Ye Xue Za Zhi; 1999 Dec; 20(12):640-2. PubMed ID: 11721367
[TBL] [Abstract][Full Text] [Related]
20. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
Sinclair P; Harrison CJ; Jarosová M; Foroni L
Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
