196 related articles for article (PubMed ID: 10629588)
1. Two cases of myeloid disorders and a t(8;12) (q12;p13).
Hernández JM; González MB; García JL; Ferro MT; Gutiérrez NC; Marynen P; San Miguel JF
Haematologica; 2000 Jan; 85(1):31-4. PubMed ID: 10629588
[TBL] [Abstract][Full Text] [Related]
2. Clonal eosinophils are a morphologic hallmark of ETV6/ABL1 positive acute myeloid leukemia.
La Starza R; Trubia M; Testoni N; Ottaviani E; Belloni E; Crescenzi B; Martelli M; Flandrin G; Pelicci PG; Mecucci C
Haematologica; 2002 Aug; 87(8):789-94. PubMed ID: 12161353
[TBL] [Abstract][Full Text] [Related]
3. Identification of new translocations involving ETV6 in hematologic malignancies by fluorescence in situ hybridization and spectral karyotyping.
Odero MD; Carlson K; Calasanz MJ; Lahortiga I; Chinwalla V; Rowley JD
Genes Chromosomes Cancer; 2001 Jun; 31(2):134-42. PubMed ID: 11319801
[TBL] [Abstract][Full Text] [Related]
4. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.
Murga Penas EM; Cools J; Algenstaedt P; Hinz K; Seeger D; Schafhausen P; Schilling G; Marynen P; Hossfeld DK; Dierlamm J
Genes Chromosomes Cancer; 2003 May; 37(1):79-83. PubMed ID: 12661008
[TBL] [Abstract][Full Text] [Related]
5. Three-way complex translocations in infant acute myeloid leukemia with t(7;12)(q36;p13): the incidence and correlation of a HLXB9 overexpression.
Park J; Kim M; Lim J; Kim Y; Han K; Lee J; Chung NG; Cho B; Kim HK
Cancer Genet Cytogenet; 2009 Jun; 191(2):102-5. PubMed ID: 19446746
[TBL] [Abstract][Full Text] [Related]
6. Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia.
Tosi S; Hughes J; Scherer SW; Nakabayashi K; Harbott J; Haas OA; Cazzaniga G; Biondi A; Kempski H; Kearney L
Genes Chromosomes Cancer; 2003 Oct; 38(2):191-200. PubMed ID: 12939747
[TBL] [Abstract][Full Text] [Related]
7. Fluorescence in situ hybridization analyses of hematologic malignancies reveal frequent cytogenetically unrecognized 12p rearrangements.
Andreasson P; Johansson B; Billström R; Garwicz S; Mitelman F; Höglund M
Leukemia; 1998 Mar; 12(3):390-400. PubMed ID: 9529134
[TBL] [Abstract][Full Text] [Related]
8. Molecular cytogenetic characterization of rearrangements involving 12p in leukemia.
Vieira L; Marques B; Cavaleiro C; Ambrósio AP; Jorge M; Neto A; Costa JM; Júnior EC; Boavida MG
Cancer Genet Cytogenet; 2005 Mar; 157(2):134-9. PubMed ID: 15721634
[TBL] [Abstract][Full Text] [Related]
9. [Report of a case of hybrid acute leukemia with t (12; 22) and literature review].
Hu XX; Gong SL; Song XM; Chen L; Qiu HY; Gao L; Wang JM
Zhonghua Xue Ye Xue Za Zhi; 2006 May; 27(5):331-4. PubMed ID: 16875585
[TBL] [Abstract][Full Text] [Related]
10. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. 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]
13. 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]
14. Heterogeneity of PLAG1 gene rearrangements in pleomorphic adenoma.
Kandasamy J; Smith A; Diaz S; Rose B; O'Brien C
Cancer Genet Cytogenet; 2007 Aug; 177(1):1-5. PubMed ID: 17693184
[TBL] [Abstract][Full Text] [Related]
15. [Abnormalities of chromosome 17 in myeloid malignancies with complex chromosomal abnormalities].
Zhu Y; Xu W; Liu Q; Pan J; Qiu H; Wang R; Qiao C; Jiang Y; Zhang S; Fan L; Zhang J; Shen Y; Xue Y; Li J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):579-82. PubMed ID: 18841577
[TBL] [Abstract][Full Text] [Related]
16. Biallelic ETV6 rearrangements by recurrent translocations t(7;12)(p15;p13) and t(3;12)(q26.2;p13) in acute myeloid leukemia.
Yamamoto K; Yakushijin K; Funakoshi Y; Inui Y; Okamura A; Matsuoka H; Minami H
Leuk Res; 2011 Nov; 35(11):e212-4. PubMed ID: 21803420
[No Abstract] [Full Text] [Related]
17. Duplication of the der(13)t(12;13)(p13;q14) in chronic myelomonocytic leukemia.
Fugazza G; Cerri R; Bruzzone R; Patrone F; Sessarego M
Haematologica; 1997; 82(3):336-7. PubMed ID: 9234584
[TBL] [Abstract][Full Text] [Related]
18. ETV6/GOT1 fusion in a case of t(10;12)(q24;p13)-positive myelodysplastic syndrome.
Struski S; Mauvieux L; Gervais C; Hélias C; Liu KL; Lessard M
Haematologica; 2008 Mar; 93(3):467-8. PubMed ID: 18310541
[TBL] [Abstract][Full Text] [Related]
19. [Identification of chromosome 21 anomalies in patients with acute myeloid leukemia by fluorescence in situ hybridization].
Zhang LJ; Wang PP; Lu XL; He J; Li Y; Zhai M
Zhonghua Yi Xue Za Zhi; 2006 Dec; 86(48):3393-6. PubMed ID: 17313849
[TBL] [Abstract][Full Text] [Related]
20. Partial duplication of the MLL oncogene in patients with aggressive acute myeloid leukemia.
Sambani C; La Starza R; Roumier C; Crescenzi B; Stavropoulou C; Katsarou O; Karafoulidou A; Dhalle JH; Lai JL; Preudhomme C; Martelli MF; Mecucci C
Haematologica; 2004 Apr; 89(4):403-7. PubMed ID: 15075073
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]