250 related articles for article (PubMed ID: 8242604)
21. Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.
Alkan M; Ramelli GP; Hirsiger H; Keser I; Remonda L; Bühler EM; Moser H
Genet Couns; 2002; 13(2):151-6. PubMed ID: 12150215
[TBL] [Abstract][Full Text] [Related]
22. Translocation (8;12;21)(q22.1;q24.1;q22.1): a new masked type of t(8;21)(q22;q22) in a patient with acute myeloid leukemia.
Saitoh K; Miura I; Ohshima A; Takahashi N; Kume M; Utsumi S; Kobayashi Y; Hashimoto K; Hatano Y; Nimura T; Saito M; Enomoto K; Ohhira M; Shimizu K; Ohki M; Miura AB
Cancer Genet Cytogenet; 1997 Jul; 96(2):111-4. PubMed ID: 9216716
[TBL] [Abstract][Full Text] [Related]
23. Cytogenetic studies in de novo acute nonlymphocytic leukemia.
Wei CH; Luh YM; Liu JH; Fan S; Hsieh RK; Chiou TJ; Tzeng CH; Chen PM
Zhonghua Yi Xue Za Zhi (Taipei); 1995 Apr; 55(4):296-301. PubMed ID: 7796356
[TBL] [Abstract][Full Text] [Related]
24. Loss of genetic material is more common than gain in acute myeloid leukemia with complex aberrant karyotype: a detailed analysis of 125 cases using conventional chromosome analysis and fluorescence in situ hybridization including 24-color FISH.
Schoch C; Haferlach T; Bursch S; Gerstner D; Schnittger S; Dugas M; Kern W; Löffler H; Hiddemann W
Genes Chromosomes Cancer; 2002 Sep; 35(1):20-9. PubMed ID: 12203786
[TBL] [Abstract][Full Text] [Related]
25. Molecular cytogenetic investigations in a novel complex variant of t(8;21)(q22;q22) with ins(15;21)(q15;q22.2q22.3) in a patient with AML-M2 subtype.
Kokate P; Ahmad F; Dalvi R; Das BR; Mandava S
Cancer Genet Cytogenet; 2008 Jul; 184(1):52-6. PubMed ID: 18558290
[TBL] [Abstract][Full Text] [Related]
26. Two distinct loci on the short arm of chromosome 16 are involved in myeloid leukemia.
Wessels JW; Mollevanger P; Dauwerse JG; Cluitmans FH; Breuning MH; Beverstock GC
Blood; 1991 Apr; 77(7):1555-9. PubMed ID: 2009371
[TBL] [Abstract][Full Text] [Related]
27. High frequency of dicentric chromosomes detected by multi-centromeric FISH in patients with acute myeloid leukemia and complex karyotype.
Sarova I; Brezinova J; Zemanova Z; Ransdorfova S; Svobodova K; Izakova S; Pavlistova L; Lizcova L; Berkova A; Skipalova K; Hodanova L; Salek C; Jonasova A; Michalova K
Leuk Res; 2018 May; 68():85-89. PubMed ID: 29574397
[TBL] [Abstract][Full Text] [Related]
28. t(16;21)(p11.2;q22): a recurrent primary rearrangement in ANLL.
Morgan R; Riske CB; Meloni A; Ries CA; Johnson CH; Lemons RS; Sandberg AA
Cancer Genet Cytogenet; 1991 May; 53(1):83-90. PubMed ID: 2036642
[TBL] [Abstract][Full Text] [Related]
29. t(8;21;8)(p23;q22;q22): a new variant form of t(8;21) translocation in acute myeloblastic leukemia with maturation.
Xue Y; Xu L; Chen S; Fu J; Guo Y; Li J; Wu Y; Pan J; Lu D
Leuk Lymphoma; 2001 Jul; 42(3):533-7. PubMed ID: 11699421
[TBL] [Abstract][Full Text] [Related]
30. A patient with de novo AML M1 and t(16;21) with karyotype evolution.
Zatkova A; Fonatsch C; Sperr WR; Valent P
Leuk Res; 2007 Sep; 31(9):1319-21. PubMed ID: 17126398
[No Abstract] [Full Text] [Related]
31. 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]
32. Discordant detection of monosomy 7 by GTG-banding and FISH in a patient with Shwachman-Diamond syndrome without evidence of myelodysplastic syndrome or acute myelogenous leukemia.
Sokolic RA; Ferguson W; Mark HF
Cancer Genet Cytogenet; 1999 Dec; 115(2):106-13. PubMed ID: 10598142
[TBL] [Abstract][Full Text] [Related]
33. Partial chromosome 21 amplification in a child with acute lymphoblastic leukemia.
Le Coniat M; Romana SP; Berger R
Genes Chromosomes Cancer; 1995 Nov; 14(3):204-9. PubMed ID: 8589037
[TBL] [Abstract][Full Text] [Related]
34. Isolation of a yeast artificial chromosome spanning the 8;21 translocation breakpoint t(8;21)(q22;q22.3) in acute myelogenous leukemia.
Gao J; Erickson P; Gardiner K; Le Beau MM; Diaz MO; Patterson D; Rowley JD; Drabkin HA
Proc Natl Acad Sci U S A; 1991 Jun; 88(11):4882-6. PubMed ID: 2052570
[TBL] [Abstract][Full Text] [Related]
35. A novel t(7;21)(q32;q22) translocation disrupting the RUNX1 gene in an adult patient with acute myeloid leukemia.
Angelova S; Zechev J; Stoimenov A; Spassov B; Romanova M; Shivarov V
Leuk Lymphoma; 2011 Dec; 52(12):2396-8. PubMed ID: 21749308
[No Abstract] [Full Text] [Related]
36. Dual color FISH on CBF primary acute myeloid leukemia.
Sorour A; Nafea D
Egypt J Immunol; 2008; 15(2):25-31. PubMed ID: 20306685
[TBL] [Abstract][Full Text] [Related]
37. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
Ballif BC; Wakui K; Gajecka M; Shaffer LG
Hum Genet; 2004 Jan; 114(2):198-206. PubMed ID: 14579147
[TBL] [Abstract][Full Text] [Related]
38. [Clinical and experimental studies on five cases of acute myeloid leukemia with translocation t(16;21)(p11;q22)].
Wu Y; Xue Y; Pan J; Ma Q
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Apr; 20(2):171-3. PubMed ID: 12673593
[TBL] [Abstract][Full Text] [Related]
39. Spectral karyotyping and fluorescence in situ hybridization analyses identified a novel three-way translocation involving inversion 16 in therapy-related acute myeloid leukemia M4eo.
Ohsaka A; Otsubo K; Yokota H; Hisa T; Saito H; Kozaki T
Cancer Genet Cytogenet; 2008 Jul; 184(2):113-8. PubMed ID: 18617061
[TBL] [Abstract][Full Text] [Related]
40. Complex chromosome translocations of standard t(8;21) and t(15;17) arise from a two-step mechanism as evidenced by fluorescence in situ hybridization analysis.
Calabrese G; Min T; Stuppia L; Powles R; Swansbury JG; Morizio E; Peila R; Donti E; Fioritoni G; Palka G
Cancer Genet Cytogenet; 1996 Oct; 91(1):40-5. PubMed ID: 8908165
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
