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Journal Abstract Search

240 related items for PubMed ID: 18000384

  • 1. DNA profiling by arrayCGH in acute myeloid leukemia and myelodysplastic syndromes.
    Suela J, Alvarez S, Cigudosa JC.
    Cytogenet Genome Res; 2007; 118(2-4):304-9. PubMed ID: 18000384
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  • 2. Translocations involving 6p22 in acute myeloid leukaemia at relapse: breakpoint characterization using microarray-based comparative genomic hybridization.
    Tchinda J, Dijkhuizen T, Vlies Pv Pv, Kok K, Horst J.
    Br J Haematol; 2004 Aug; 126(4):495-500. PubMed ID: 15287941
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  • 3. Molecular characterisation of a recurrent, semi-cryptic RUNX1 translocation t(7;21) in myelodysplastic syndrome and acute myeloid leukaemia.
    Foster N, Paulsson K, Sales M, Cunningham J, Groves M, O'Connor N, Begum S, Stubbs T, McMullan DJ, Griffiths M, Pratt N, Tauro S.
    Br J Haematol; 2010 Mar; 148(6):938-43. PubMed ID: 20064152
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  • 4. Single nucleotide polymorphism array-based karyotyping in acute myeloid leukemia or myelodysplastic syndrome with trisomy 8 as the sole chromosomal abnormality.
    Hahm C, Mun YC, Seong CM, Han SH, Chung WS, Huh J.
    Acta Haematol; 2013 Mar; 129(3):154-8. PubMed ID: 23208021
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  • 5. Molecular cytogenetic profiling of complex karyotypes in primary myelodysplastic syndromes and acute myeloid leukemia.
    Trost D, Hildebrandt B, Beier M, Müller N, Germing U, Royer-Pokora B.
    Cancer Genet Cytogenet; 2006 Feb; 165(1):51-63. PubMed ID: 16490597
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  • 6. Translocation (7;9)(q22;q34) in therapy-related myelodysplastic syndrome after allogeneic bone marrow transplantation for acute myeloblastic leukemia.
    Yamamoto K, Yakushijin K, Kawamori Y, Minagawa K, Katayama Y, Matsui T.
    Cancer Genet Cytogenet; 2007 Jul 01; 176(1):61-6. PubMed ID: 17574966
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  • 14. AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes.
    Zatkova A, Merk S, Wendehack M, Bilban M, Muzik EM, Muradyan A, Haferlach C, Haferlach T, Wimmer K, Fonatsch C, Ullmann R.
    Genes Chromosomes Cancer; 2009 Jun 01; 48(6):510-20. PubMed ID: 19306356
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  • 16. Single nucleotide polymorphism array-based karyotyping shows sequential genomic changes from monosomy to copy-neutral loss of heterozygosity of chromosome 7 and 20q deletion within a balanced translocation t(14;20) in AML.
    Huh J, Mun YC, Seong CM, Chung WS.
    Cancer Genet; 2011 Dec 01; 204(12):682-6. PubMed ID: 22285021
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  • 17. 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 01; 145(2):190-7. PubMed ID: 19222471
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  • 18. Centromeric breakage and highly rearranged chromosome derivatives associated with mutations of TP53 are common in therapy-related MDS and AML after therapy with alkylating agents: an M-FISH study.
    Andersen MK, Christiansen DH, Pedersen-Bjergaard J.
    Genes Chromosomes Cancer; 2005 Apr 01; 42(4):358-71. PubMed ID: 15645489
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