232 related articles for article (PubMed ID: 16875944)
1. PML/RARA rearrangement associated with a t(15;19;17) in a case of acute myeloid leukemia with abundant myelocytes with salmon-pink cytoplasm.
Kim IS; Kim HJ; Choung HS; Jung CW; Kim JW; Kim SH
Cancer Genet Cytogenet; 2006 Aug; 169(1):81-2. PubMed ID: 16875944
[No Abstract] [Full Text] [Related]
2. Derivative (7)t(7;8): The sole karyotype abnormality in acute promyelocytic leukemia with PML/RARA rearrangement identified by RT-PCR and sequence analysis.
Wang Y; Fang M; Jing Y; Li J; Jiang F; Wang Y
Leuk Res; 2009 Jul; 33(7):e55-8. PubMed ID: 19162322
[No Abstract] [Full Text] [Related]
3. Variant acute promyelocytic leukemia translocation (15;17) originating from two subsequent balanced translocations involving the same chromosomes 15 and 17 while preserving the PML/RARA fusion.
Tirado CA; Jahn JA; Scheerle J; Eid M; Meister RJ; Christie RJ; Croft CD; Wallingford S; Heritage DW; Mowrey PN; Meloni-Ehrig AM
Cancer Genet Cytogenet; 2005 Aug; 161(1):70-3. PubMed ID: 16080960
[TBL] [Abstract][Full Text] [Related]
4. A t(17;20)(q21;q12) masking a variant t(15;17)(q22;q21) in a patient with acute promyelocytic leukemia.
García-Casado Z; Cervera J; Valencia A; Pajuelo JC; Mena-Duran AV; Barragán E; Bolufer P; Sanz MA
Cancer Genet Cytogenet; 2006 Jul; 168(1):73-6. PubMed ID: 16772124
[TBL] [Abstract][Full Text] [Related]
5. Cryptic insertion (15;17) in a case of acute promyelocytic leukemia detected by fluorescence in situ hybridization.
Gutiérrez NC; García JL; Chillón C; Muntión S; González M; Hernández JM
Haematologica; 1999 Jan; 84(1):88-90. PubMed ID: 10091399
[No Abstract] [Full Text] [Related]
6. [Detection of PML/RARA rearrangement by reverse transcriptase-PCR and sequencing in a case of microgranular acute promyelocytic leukemia lacking t(15;17) on karyotype and FISH].
Kim KE; Woo KS; Kim SH; Han JY
Korean J Lab Med; 2009 Oct; 29(5):379-83. PubMed ID: 19893344
[TBL] [Abstract][Full Text] [Related]
7. A new complex translocation t(5;17;15)(q11;q21;q22) in acute promyelocytic leukemia.
Abe S; Ishikawa I; Harigae H; Sugawara T
Cancer Genet Cytogenet; 2008 Jul; 184(1):44-7. PubMed ID: 18558288
[TBL] [Abstract][Full Text] [Related]
8. Secondary near-tetraploidy with double der(15)t(15;17) in acute promyelocytic leukemia in relapse.
Morita Y; Takahashi A; Yamamoto K; Miki T; Murakami N; Miura O
Cancer Genet Cytogenet; 2004 Mar; 149(2):131-6. PubMed ID: 15036889
[TBL] [Abstract][Full Text] [Related]
9. Case report: acute promyelocytic leukemia with +der(17)t(15;17) detected by fluorescence in situ hybridization (FISH).
Kim M; Lim J; Kim Y; Han K; Lee S; Min CK
Ann Clin Lab Sci; 2005; 35(2):195-8. PubMed ID: 15943185
[TBL] [Abstract][Full Text] [Related]
10. Cryptic t(15;17) in a patient with AML M3 and a complex karyotype.
Göhring G; Lange K; Atta J; Krauter J; Hölzer D; Schlegelberger B
Cancer Genet Cytogenet; 2007 May; 175(1):77-80. PubMed ID: 17498564
[No Abstract] [Full Text] [Related]
11. A new variant t(6;15;17)(q25;q22;q21) in acute promyelocytic leukemia: fluorescence in situ hybridization confirmation.
Eclache V; Viguie F; Frocrain C; Cassinat B; Chomienne C; Cymbalista F; Fenaux P
Cancer Genet Cytogenet; 2005 May; 159(1):69-73. PubMed ID: 15860361
[TBL] [Abstract][Full Text] [Related]
12. Cytogenetically cryptic and FISH-negative PML/RARA rearrangement in acute promyelocytic leukemia detected only by PCR: an exceedingly rare phenomenon.
Blanco EM; Curry CV; Lu XY; Sarabia SF; Redell MS; Lopez-Terrada DH; Roy A
Cancer Genet; 2014; 207(1-2):48-9. PubMed ID: 24561214
[No Abstract] [Full Text] [Related]
13. Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98-C6orf80 fusion in a case of acute megakaryoblastic leukemia.
Tosi S; Ballabio E; Teigler-Schlegel A; Boultwood J; Bruch J; Harbott J
Genes Chromosomes Cancer; 2005 Nov; 44(3):225-32. PubMed ID: 16028218
[TBL] [Abstract][Full Text] [Related]
14. Cryptic translocation of PML/RARA on 17q. A rare event in acute promyelocytic leukemia.
Zaccaria A; Valenti A; Toschi M; Salvucci M; Cipriani R; Ottaviani E; Martinelli G
Cancer Genet Cytogenet; 2002 Oct; 138(2):169-73. PubMed ID: 12505266
[TBL] [Abstract][Full Text] [Related]
15. [Translocation t(6;9;8)(p23;q34;q22) in acute myeloid leukemia: Contribution of fluorescence in situ hybridization].
van den Akker J; Pérot C; Portnoï MF; Philizot L; Dupont JM; Laporte JP; Taillemite JL
Ann Genet; 1995; 38(3):168-71. PubMed ID: 8540689
[TBL] [Abstract][Full Text] [Related]
16. Two new molecular PML-RARalpha variants: implications for the molecular diagnosis of APL.
Vizmanos JL; Larrráyoz MJ; Odero MD; Lasa R; González M; Novo FJ; Calasanz MJ
Haematologica; 2002 Aug; 87(8):ELT37. PubMed ID: 12161382
[No Abstract] [Full Text] [Related]
17. Therapy-related acute myeloid leukemia after successful therapy for acute promyelocytic leukemia with t(15;17): A case report and literature review.
Bao L; Lu X; Lai Y; Zhang X; Zhu H; Liu Y; Qin Y; Huang XJ
Leuk Res; 2009 Jul; 33(7):e64-8. PubMed ID: 19297021
[No Abstract] [Full Text] [Related]
18. Acquired Robertsonian translocations in leukemia: two more cases.
Herring DB; Harbert KA; Wenger SL; Ericson SG
Cancer Genet Cytogenet; 2005 Apr; 158(2):196-7. PubMed ID: 15796971
[No Abstract] [Full Text] [Related]
19. NUP98 is fused to topoisomerase (DNA) IIbeta 180 kDa (TOP2B) in a patient with acute myeloid leukemia with a new t(3;11)(p24;p15).
Nebral K; Schmidt HH; Haas OA; Strehl S
Clin Cancer Res; 2005 Sep; 11(18):6489-94. PubMed ID: 16166424
[TBL] [Abstract][Full Text] [Related]
20. NUP98-NSD1 fusion by insertion in acute myeloblastic leukemia.
Petit A; Radford I; Waill MC; Romana S; Berger R
Cancer Genet Cytogenet; 2008 Jan; 180(1):43-6. PubMed ID: 18068532
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
