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172 related items for PubMed ID: 14580777
1. Detection of cryptic MLL insertions using a commercial dual-color fluorescence in situ hybridization probe. Dyson MJ, Talley PJ, Reilly JT, Stevenson D, Parsons E, Tighe J. Cancer Genet Cytogenet; 2003 Nov; 147(1):81-3. PubMed ID: 14580777 [Abstract] [Full Text] [Related]
2. Cryptic insertion and translocation or nondividing leukemic cells disclosed by FISH analysis in infant acute leukemia with discrepant molecular and cytogenetic findings. Watanabe N, Kobayashi H, Ichiji O, Yoshida MA, Kikuta A, Komada Y, Sekine I, Ishida Y, Horiukoshi Y, Tsunematsu Y, Yano M, Nakadate H, Kaneko Y. Leukemia; 2003 May; 17(5):876-82. PubMed ID: 12750700 [Abstract] [Full Text] [Related]
3. A DNA probe combination for improved detection of MLL/11q23 breakpoints by double-color interphase-FISH in acute leukemias. von Bergh A, Emanuel B, van Zelderen-Bhola S, Smetsers T, van Soest R, Stul M, Vranckx H, Schuuring E, Hagemeijer A, Kluin P. Genes Chromosomes Cancer; 2000 May; 28(1):14-22. PubMed ID: 10738298 [Abstract] [Full Text] [Related]
4. Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5. Poirel H, Rack K, Delabesse E, Radford-Weiss I, Troussard X, Debert C, Leboeuf D, Bastard C, Picard F, Veil-Buzyn A, Flandrin G, Bernard O, Macintyre E. Blood; 1996 Mar 15; 87(6):2496-505. PubMed ID: 8630416 [Abstract] [Full Text] [Related]
5. Jumping translocation at 11q23 with MLL gene rearrangement and interstitial telomeric sequences. Cuthbert G, McCullough S, Finney R, Breese G, Bown N. Genes Chromosomes Cancer; 1999 Apr 15; 24(4):295-8. PubMed ID: 10092126 [Abstract] [Full Text] [Related]
6. [Study on mixed lineage leukemia gene rearrangement in AML-M4/M5 by interphase fluorescence in situ hybridization]. Pan JL, Xue YQ, Jiang HY, Li JY, Chen SN, Wu YF. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Jun 15; 21(3):288-90. PubMed ID: 15192841 [Abstract] [Full Text] [Related]
7. Cryptic 5' MLL gene insertion in an X-chromosome in acute myeloblastic leukemia. Douet-Guilbert N, Arnaud B, Morel F, Le Bris MJ, De Braekeleer M. Cancer Genet Cytogenet; 2005 Mar 15; 157(2):178-80. PubMed ID: 15721643 [Abstract] [Full Text] [Related]
9. Clinical and biological characteristics of adult de novo and secondary acute myeloid leukemia with balanced 11q23 chromosomal anomaly or MLL gene rearrangement compared to cases with unbalanced 11q23 anomaly: confirmation of the existence of different entities with 11q23 breakpoint. Archimbaud E, Charrin C, Magaud JP, Campos L, Thomas X, Fière D, Rimokh R. Leukemia; 1998 Jan 15; 12(1):25-33. PubMed ID: 9436917 [Abstract] [Full Text] [Related]
10. MLL/SEPTIN6 chimeric transcript from inv ins(X;11)(q24;q23q13) in acute monocytic leukemia: report of a case and review of the literature. Kim HJ, Ki CS, Park Q, Koo HH, Yoo KH, Kim EJ, Kim SH. Genes Chromosomes Cancer; 2003 Sep 15; 38(1):8-12. PubMed ID: 12874781 [Abstract] [Full Text] [Related]
11. Amplification of the 11q23 region in acute myeloid leukemia. Avet-Loiseau H, Godon C, Li JY, Daviet A, Mellerin MP, Talmant P, Harousseau JL, Bataille R. Genes Chromosomes Cancer; 1999 Oct 15; 26(2):166-70. PubMed ID: 10469455 [Abstract] [Full Text] [Related]
12. Routine fluorescence in situ hybridization with the MLL probe does not reliably detect two separate signals on one chromosome 11 in patients with trisomy 11. Smith A, Robson L, Heaps LS, Sharma P, Dunlop L, Bhave A, Bradstock K. Cancer Genet Cytogenet; 2001 Sep 15; 129(2):173-6. PubMed ID: 11566351 [Abstract] [Full Text] [Related]
13. Screening by fluorescence in situ hybridization for MLL status at diagnosis in 239 unselected patients with acute myeloblastic leukemia. Arnaud B, Douet-Guilbert N, Morel F, Le Bris MJ, Herry A, Banzakour S, Bourquard P, Morice P, Le Calvez G, Marion V, Abgrall JF, Berthou C, De Braekeleer M. Cancer Genet Cytogenet; 2005 Sep 15; 161(2):110-5. PubMed ID: 16102580 [Abstract] [Full Text] [Related]
14. Variations in MLL amplification in a patient with acute myeloid leukemia. Brezinová J, Zemanová Z, Cermák J, Kurková S, Sindelárová L, Schwarz J, Michalová K. Leuk Lymphoma; 2002 Oct 15; 43(10):2031-5. PubMed ID: 12481904 [Abstract] [Full Text] [Related]
16. Incidence of MLL rearrangement in acute myeloid leukemia, and a CALM-AF10 fusion in M4 type acute myeloblastic leukemia. Abdou SM, Jadayel DM, Min T, Swansbury GJ, Dainton MG, Jafer O, Powles RL, Catovsky D. Leuk Lymphoma; 2002 Jan 15; 43(1):89-95. PubMed ID: 11911106 [Abstract] [Full Text] [Related]
17. Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia. Super HG, Strissel PL, Sobulo OM, Burian D, Reshmi SC, Roe B, Zeleznik-Le NJ, Diaz MO, Rowley JD. Genes Chromosomes Cancer; 1997 Oct 15; 20(2):185-95. PubMed ID: 9331569 [Abstract] [Full Text] [Related]
18. Granulocytic sarcoma in MLL-positive infant acute myelogenous leukemia: fluorescence in situ hybridization study of childhood acute myelogenous leukemia for detecting MLL rearrangement. Park KU, Lee DS, Lee HS, Kim CJ, Cho HI. Am J Pathol; 2001 Dec 15; 159(6):2011-6. PubMed ID: 11733351 [Abstract] [Full Text] [Related]
19. Frequency and clinical significance of the MLL gene rearrangements in infant acute leukemia. Taki T, Ida K, Bessho F, Hanada R, Kikuchi A, Yamamoto K, Sako M, Tsuchida M, Seto M, Ueda R, Hayashi Y. Leukemia; 1996 Aug 15; 10(8):1303-7. PubMed ID: 8709635 [Abstract] [Full Text] [Related]
20. X chromosome insertion in the MLL gene in a case of childhood acute myeloblastic leukemia. Arnaud B, Morel F, Douet-Guilbert N, Le Bris MJ, De Braekeleer M. Cancer Genet Cytogenet; 2004 Jul 15; 152(2):149-52. PubMed ID: 15262436 [Abstract] [Full Text] [Related] Page: [Next] [New Search]