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Journal Abstract Search

761 related items for PubMed ID: 10598142

  • 1. 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
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  • 2. Malignant myeloid transformation with isochromosome 7q in Shwachman-Diamond syndrome.
    Dror Y, Squire J, Durie P, Freedman MH.
    Leukemia; 1998 Oct; 12(10):1591-5. PubMed ID: 9766504
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  • 3. Chromosome 20q deletion and progression to monosomy 7 in a patient with Shwachman-Diamond syndrome without MDS/AML.
    Raj AB, Bertolone SJ, Barch MJ, Hersh JH.
    J Pediatr Hematol Oncol; 2003 Jun; 25(6):508-9. PubMed ID: 12794535
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  • 6. Does monosomy 5 really exist in myelodysplastic syndromes and acute myeloid leukemia?
    Galván AB, Mallo M, Arenillas L, Salido M, Espinet B, Pedro C, Florensa L, Serrano S, Solé F.
    Leuk Res; 2010 Sep; 34(9):1242-5. PubMed ID: 20362335
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  • 9. The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.
    Maserati E, Pressato B, Valli R, Minelli A, Sainati L, Patitucci F, Marletta C, Mastronuzzi A, Poli F, Lo Curto F, Locatelli F, Danesino C, Pasquali F.
    Br J Haematol; 2009 Apr; 145(2):190-7. PubMed ID: 19222471
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  • 10. Application of FISH 7q in MDS patients without monosomy 7 or 7q deletion by conventional G-banding cytogenetics: does -7/7q- detection by FISH have prognostic value?
    Ademà V, Hernández JM, Abáigar M, Lumbreras E, Such E, Calull A, Dominguez E, Arenillas L, Mallo M, Cervera J, Marugán I, Tormo M, García F, González T, Luño E, Sanzo C, Martín ML, Fernández M, Costa D, Blázquez B, Barreña B, Marco F, Batlle A, Buño I, Martínez-Laperche C, Noriega V, Collado R, Ivars D, Carbonell F, Vallcorba I, Melero J, Delgado E, Vargas MT, Grau J, Salido M, Espinet B, Melero C, Florensa L, Pedro C, Solé F.
    Leuk Res; 2013 Apr; 37(4):416-21. PubMed ID: 23337401
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  • 12. Numerical chromosomal changes and risk of development of myelodysplastic syndrome--acute myeloid leukemia in patients with Fanconi anemia.
    Mehta PA, Harris RE, Davies SM, Kim MO, Mueller R, Lampkin B, Mo J, Myers K, Smolarek TA.
    Cancer Genet Cytogenet; 2010 Dec; 203(2):180-6. PubMed ID: 21156231
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  • 13. A multimodal approach in the diagnosis of patients with hematopoietic disorders.
    Mark HF, Gray Y, Mark Y, Khorsand J, Sikov W.
    Cancer Genet Cytogenet; 1999 Feb; 109(1):14-20. PubMed ID: 9973954
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  • 15. Chromosomal aberrations in congenital bone marrow failure disorders--an early indicator for leukemogenesis?
    Göhring G, Karow A, Steinemann D, Wilkens L, Lichter P, Zeidler C, Niemeyer C, Welte K, Schlegelberger B.
    Ann Hematol; 2007 Oct; 86(10):733-9. PubMed ID: 17653548
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  • 16. Possible evidence for genomic imprinting in childhood acute myeloblastic leukaemia associated with monosomy for chromosome 7.
    Katz F, Webb D, Gibbons B, Reeves B, McMahon C, Chessells J, Mitchell C.
    Br J Haematol; 1992 Mar; 80(3):332-6. PubMed ID: 1581212
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  • 19. Comparison of I-FISH and G-banding for the detection of chromosomal abnormalities during the evolution of myelodysplastic syndrome.
    Pinheiro RF, Chauffaille ML.
    Braz J Med Biol Res; 2009 Nov; 42(11):1110-2. PubMed ID: 19855907
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  • 20. [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
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