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Journal Abstract Search

116 related items for PubMed ID: 1555197

  • 1. del(16)(q22) in a child with acute myeloid leukemia without bone marrow eosinophilia.
    Kawachi T, Nakamura H, Sadamori N, Tomonaga M, Kamihira S, Maeda H, Tsuji Y.
    Cancer Genet Cytogenet; 1992 Mar; 59(1):86-8. PubMed ID: 1555197
    [No Abstract] [Full Text] [Related]

  • 2. A myelodysplastic syndrome with marrow eosinophilia terminating in acute nonlymphocytic leukemia, associated with an abnormal chromosome 16.
    Abbondanzo SL, Gray RG, Whang-Peng J, Jacobson RJ.
    Arch Pathol Lab Med; 1987 Apr; 111(4):330-2. PubMed ID: 3469939
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  • 3. Interstitial deletion del(7)(q22;q31) in a case of Ph-negative CML.
    Turchini MF, Geneix A, François P, De Larocque A, Malet P.
    Cancer Genet Cytogenet; 1985 Jan 01; 14(1-2):179-81. PubMed ID: 3855273
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  • 4. Acute myelomonocytic leukemia with marrow eosinophilia showing 5q- and 16q22 mosaicism.
    Hamamoto K, Yoshioka A, Taniguchi H, Ohaga S, Nagano T, Kishimoto Y, Kitajima H, Fujimoto M, Kimura T, Fujitake H.
    Cancer Genet Cytogenet; 1992 Feb 01; 58(2):130-3. PubMed ID: 1551075
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  • 7. Two different karyotypes with 1q abnormalities in a patient with Fanconi anemia.
    Oliveira NI, Ribeiro EM, Raimondi SC, Bittencourt MA, Pasquini R, Cavalli IJ.
    Leuk Res; 2002 Nov 01; 26(11):1047-9. PubMed ID: 12363475
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  • 8. Coexistent t(8;21)(q22;q22) Translocation and 5q Deletion in Acute Myeloid Leukemia.
    Yamamoto K, Yakushijin K, Sanada Y, Kawamoto S, Matsuoka H, Minami H.
    J Clin Exp Hematop; 2015 Nov 01; 55(3):181-5. PubMed ID: 26763368
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  • 9. Chronic myelomonocytic leukemia with trisomy 8 and a related clone with trisomy 8 and t(15;17).
    Dalton WT, Cork A, Stass SA, Trujillo JM.
    Cancer Genet Cytogenet; 1988 Jun 01; 32(2):287-92. PubMed ID: 3163267
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  • 10. Partial deletion of long arm of chromosome 17: a specific abnormality in acute promyelocytic leukemia?
    Golomb HM, Rowley J, Vardiman J, Baron J, Locker G, Krasnow S.
    Arch Intern Med; 1976 Jul 01; 136(7):825-8. PubMed ID: 1065255
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  • 12. Interstitial deletion of the long arm of chromosome 9 as the sole anomaly in acute myeloid leukaemia is associated with dyserythropoiesis.
    Kwong YL, Chan TK, Chan LC.
    Leukemia; 1992 Jan 01; 6(1):64-5. PubMed ID: 1736015
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  • 15. Philadelphia-positive acute myelomonocytic leukemia with inversion of chromosome 16 and eosinobasophils.
    Mecucci C, Noens L, Aventin A, Testoni N, Van den Berghe H.
    Am J Hematol; 1988 Jan 01; 27(1):69-71. PubMed ID: 3162648
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  • 16. [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 01; 20(2):171-3. PubMed ID: 12673593
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  • 18. Treatment of deletion 5q acute myeloid leukemia with lenalidomide.
    Lancet JE, List AF, Moscinski LC.
    Leukemia; 2007 Mar 01; 21(3):586-8. PubMed ID: 17230228
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  • 19. Fifty-one patients with acute myeloid leukemia and translocation t(8;21)(q22;q22): an additional deletion in 9q is an adverse prognostic factor.
    Schoch C, Haase D, Haferlach T, Gudat H, Büchner T, Freund M, Link H, Lengfelder E, Wandt H, Sauerland MC, Löffler H, Fonatsch C.
    Leukemia; 1996 Aug 01; 10(8):1288-95. PubMed ID: 8709633
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  • 20. Inv(16) abnormality and eosinophilia in a patient with acute nonlymphocytic leukemia.
    Okada M, Yamada O, Mizoguchi H, Kubota K, Nomura Y.
    Cancer Genet Cytogenet; 1985 Jan 01; 14(1-2):185-7. PubMed ID: 3965124
    [No Abstract] [Full Text] [Related]

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