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Journal Abstract Search

358 related items for PubMed ID: 9218994

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  • 27. Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques.
    Salaverria I, Espinet B, Carrió A, Costa D, Astier L, Slotta-Huspenina J, Quintanilla-Martinez L, Fend F, Solé F, Colomer D, Serrano S, Miró R, Beà S, Campo E.
    Genes Chromosomes Cancer; 2008 Dec; 47(12):1086-97. PubMed ID: 18709664
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  • 28. Stromal cells and human malignant neuroblasts derived from bone marrow metastasis may share common karyotypic abnormalities: the case of the IGR-N-91 cell line.
    Valent A, Venuat AM, Danglot G, Da Silva J, Duarte N, Bernheim A, Bénard J.
    Med Pediatr Oncol; 2001 Jan; 36(1):100-3. PubMed ID: 11464856
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  • 29. Molecular cytogenetic delineation of 17q translocation breakpoints in neuroblastoma cell lines.
    Lastowska M, Van Roy N, Bown N, Speleman F, Lunec J, Strachan T, Pearson AD, Jackson MS.
    Genes Chromosomes Cancer; 1998 Oct; 23(2):116-22. PubMed ID: 9739014
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  • 30. Loss of heterozygosity for alleles on chromosomes 11q and 14q in neuroblastoma.
    Srivatsan ES, Murali V, Seeger RC.
    Prog Clin Biol Res; 1991 Oct; 366():91-8. PubMed ID: 2068183
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  • 31. The N-myc and c-myc downstream pathways include the chromosome 17q genes nm23-H1 and nm23-H2.
    Godfried MB, Veenstra M, v Sluis P, Boon K, v Asperen R, Hermus MC, v Schaik BD, Voûte TP, Schwab M, Versteeg R, Caron HN.
    Oncogene; 2002 Mar 27; 21(13):2097-101. PubMed ID: 11960382
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  • 32. Malignant peripheral nerve sheath tumor with rhabdomyoblastic differentiation (malignant triton tumor) with balanced t(7;9)(q11.2;p24) and unbalanced translocation der(16)t(1;16)(q23;q13).
    Velagaleti GV, Miettinen M, Gatalica Z.
    Cancer Genet Cytogenet; 2004 Feb 27; 149(1):23-7. PubMed ID: 15104279
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  • 33. Comparative genomic hybridization study of primary neuroblastoma tumors. United Kingdom Children's Cancer Study Group.
    Lastowska M, Nacheva E, McGuckin A, Curtis A, Grace C, Pearson A, Bown N.
    Genes Chromosomes Cancer; 1997 Mar 27; 18(3):162-9. PubMed ID: 9071568
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  • 34. Spectral karyotyping identifies recurrent complex rearrangements of chromosomes 8, 17, and 20 in osteosarcomas.
    Bayani J, Zielenska M, Pandita A, Al-Romaih K, Karaskova J, Harrison K, Bridge JA, Sorensen P, Thorner P, Squire JA.
    Genes Chromosomes Cancer; 2003 Jan 27; 36(1):7-16. PubMed ID: 12461745
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  • 35. Novel 6p rearrangements and recurrent translocation breakpoints in retinoblastoma cell lines identified by spectral karyotyping and mBAND analyses.
    Paderova J, Orlic-Milacic M, Yoshimoto M, da Cunha Santos G, Gallie B, Squire JA.
    Cancer Genet Cytogenet; 2007 Dec 27; 179(2):102-11. PubMed ID: 18036396
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  • 36. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
    Petit P, Devriendt K, Vermeesch JR, Meireleire J, Fryns JP.
    Genet Couns; 1998 Dec 27; 9(3):215-21. PubMed ID: 9777345
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  • 37. Breakpoint position on 17q identifies the most aggressive neuroblastoma tumors.
    Łastowska M, Cotterill S, Bown N, Cullinane C, Variend S, Lunec J, Strachan T, Pearson AD, Jackson MS.
    Genes Chromosomes Cancer; 2002 Aug 27; 34(4):428-36. PubMed ID: 12112532
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  • 38. 17q gain in neuroblastoma predicts adverse clinical outcome. U.K. Cancer Cytogenetics Group and the U.K. Children's Cancer Study Group.
    Bown N, Lastowska M, Cotterill S, O'Neill S, Ellershaw C, Roberts P, Lewis I, Pearson AD, U.K. Cancer Cytogenetics Group and the U.K. Children's Cancer Study Group.
    Med Pediatr Oncol; 2001 Jan 27; 36(1):14-9. PubMed ID: 11464868
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