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121 related items for PubMed ID: 8388166

  • 1. Acute promyelocytic leukemia with the pseudo-Chediak-Higashi anomaly and molecular documentation of t(15;17) chromosomal translocation.
    Symes PH, Williams ME, Flessa HC, Srivastava AK, Swerdlow SH.
    Am J Clin Pathol; 1993 May; 99(5):622-7. PubMed ID: 8388166
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  • 2. Acute promyelocytic leukemia with additional chromosomal abnormalities and absence of Auer rods.
    Kaleem Z, Watson MS, Zutter MM, Blinder MA, Hess JL.
    Am J Clin Pathol; 1999 Jul; 112(1):113-8. PubMed ID: 10396293
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  • 4. Leukemias resembling acute promyelocytic leukemia, microgranular variant.
    Nagendra S, Meyerson H, Skallerud G, Rosenthal N.
    Am J Clin Pathol; 2002 Apr; 117(4):651-7. PubMed ID: 11939742
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  • 5. Pulsed-field gel electrophoresis analysis of retinoic acid receptor-alpha and promyelocytic leukemia rearrangements. Detection of the t(15;17) translocation in the diagnosis of acute promyelocytic leukemia.
    Xiao YH, Miller WH, Warrell RP, Dmitrovsky E, Zelenetz AD.
    Am J Pathol; 1993 Nov; 143(5):1301-11. PubMed ID: 8238249
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  • 6. Identification of signature genes by microarray for acute myeloid leukemia without maturation and acute promyelocytic leukemia with t(15;17)(q22;q12)(PML/RARalpha).
    Morikawa J, Li H, Kim S, Nishi K, Ueno S, Suh E, Dougherty E, Shmulevich I, Shiku H, Zhang W, Kobayashi T.
    Int J Oncol; 2003 Sep; 23(3):617-25. PubMed ID: 12888896
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  • 7. A new variant translocation of t(15;17) in a patient with acute promyelocytic leukemia (M3): t(15;19;17)(q22;p13;q12).
    Saitoh K, Miura I, Kobayashi Y, Kume M, Utsumi S, Takahashi N, Hatano Y, Nimura T, Hashimoto K, Takahashi S, Miura AB.
    Cancer Genet Cytogenet; 1998 Apr 01; 102(1):15-8. PubMed ID: 9530334
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  • 8. Rearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemia.
    Chen SJ, Zelent A, Tong JH, Yu HQ, Wang ZY, Derré J, Berger R, Waxman S, Chen Z.
    J Clin Invest; 1993 May 01; 91(5):2260-7. PubMed ID: 8387545
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  • 9. t(X;17) as the sole karyotypic anomaly in a case of M(3r) subtype of acute promyelocytic leukemia without RARalpha rearrangement.
    Wang HP, Xu H, Chen ZM, Tong XM, Qian WB, Jin J.
    Leuk Res; 2010 Feb 01; 34(2):e55-7. PubMed ID: 19477513
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  • 13. 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 01; 149(2):131-6. PubMed ID: 15036889
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  • 16. Molecular rearrangements of the MYL gene in acute promyelocytic leukemia (APL, M3) define a breakpoint cluster region as well as some molecular variants.
    Tong JH, Dong S, Geng JP, Huang W, Wang ZY, Sun GL, Chen SJ, Chen Z, Larsen CJ, Berger R.
    Oncogene; 1992 Feb 01; 7(2):311-6. PubMed ID: 1312695
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  • 17. Acute promyelocytic leukemia (AML-M3)--Part 2: Molecular defect, DNA diagnosis, and proposed models of leukemogenesis and differentiation therapy.
    Randolph TR.
    Clin Lab Sci; 2000 Feb 01; 13(2):106-16. PubMed ID: 11066449
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  • 18. Morphology of acute promyelocytic leukemia with cytogenetic or molecular evidence for the diagnosis: characterization of additional microgranular variants.
    Neame PB, Soamboonsrup P, Leber B, Carter RF, Sunisloe L, Patterson W, Orzel A, Bates S, McBride JA.
    Am J Hematol; 1997 Nov 01; 56(3):131-42. PubMed ID: 9371524
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  • 19. A non-classical translocation involving 17q12 (retinoic acid receptor alpha) in acute promyelocytic leukemia (APML) with atypical features.
    Corey SJ, Locker J, Oliveri DR, Shekhter-Levin S, Redner RL, Penchansky L, Gollin SM.
    Leukemia; 1994 Aug 01; 8(8):1350-3. PubMed ID: 8057672
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  • 20. Molecular heterogeneity of the PML gene rearrangement in acute promyelocytic leukemia: prevalence and clinical significance.
    Fukutani H, Naoe T, Yoshida H, Yamamori S, Ohno R.
    Jpn J Cancer Res; 1993 Mar 01; 84(3):257-64. PubMed ID: 8387477
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