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Journal Abstract Search

151 related items for PubMed ID: 8037210

  • 1. Translocation involving 1p and 17q is a recurrent genetic alteration of human neuroblastoma cells.
    Savelyeva L, Corvi R, Schwab M.
    Am J Hum Genet; 1994 Aug; 55(2):334-40. PubMed ID: 8037210
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  • 2. Analysis of 1;17 translocation breakpoints in neuroblastoma: implications for mapping of neuroblastoma genes.
    Van Roy N, Laureys G, Van Gele M, Opdenakker G, Miura R, van der Drift P, Chan A, Versteeg R, Speleman F.
    Eur J Cancer; 1997 Oct; 33(12):1974-8. PubMed ID: 9516836
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  • 3. Molecular cytogenetic analysis of 1;17 translocations in neuroblastoma.
    Van Roy N, Cheng NC, Laureys G, Opdenakker G, Versteeg R, Speleman F.
    Eur J Cancer; 1995 Oct; 31A(4):530-5. PubMed ID: 7576960
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  • 5. Promiscuous translocations of chromosome arm 17q in human neuroblastomas.
    Lastowska M, Roberts P, Pearson AD, Lewis I, Wolstenholme J, Bown N.
    Genes Chromosomes Cancer; 1997 Jul; 19(3):143-9. PubMed ID: 9218994
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  • 6. Characterisation of the chromosome breakpoints in a patient with a constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12) and neuroblastoma.
    Laureys G, Versteeg R, Speleman F, van der Drift P, Francke U, Opdenakker G, Van Roy N.
    Eur J Cancer; 1995 Jul; 31A(4):523-6. PubMed ID: 7576958
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  • 7. Stepwise occurrence of a complex unbalanced translocation in neuroblastoma leading to insertion of a telomere sequence and late chromosome 17q gain.
    Schleiermacher G, Bourdeaut F, Combaret V, Picrron G, Raynal V, Aurias A, Ribeiro A, Janoueix-Lerosey I, Delattre O.
    Oncogene; 2005 May 05; 24(20):3377-84. PubMed ID: 15735707
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  • 8. der(11)t(11;17): a distinct cytogenetic pathway of advanced stage neuroblastoma (NBL) - detected by spectral karyotyping (SKY).
    Stark B, Jeison M, Glaser-Gabay L, Bar-Am I, Mardoukh J, Ash S, Atias D, Stein J, Zaizov R, Yaniv I.
    Cancer Lett; 2003 Jul 18; 197(1-2):75-9. PubMed ID: 12880963
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  • 10. 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 18; 23(2):116-22. PubMed ID: 9739014
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  • 12. Gain of chromosome arm 17q and adverse outcome in patients with neuroblastoma.
    Bown N, Cotterill S, Lastowska M, O'Neill S, Pearson AD, Plantaz D, Meddeb M, Danglot G, Brinkschmidt C, Christiansen H, Laureys G, Speleman F, Nicholson J, Bernheim A, Betts DR, Vandesompele J, Van Roy N.
    N Engl J Med; 1999 Jun 24; 340(25):1954-61. PubMed ID: 10379019
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  • 13. Constitutional translocation t(1;17)(p36.31-p36.13;q11.2-q12.1) in a neuroblastoma patient. Establishment of somatic cell hybrids and identification of PND/A12M2 on chromosome 1 and NF1/SCYA7 on chromosome 17 as breakpoint flanking single copy markers.
    Laureys G, Speleman F, Versteeg R, van der Drift P, Chan A, Leroy J, Francke U, Opdenakker G, Van Roy N.
    Oncogene; 1995 Mar 16; 10(6):1087-93. PubMed ID: 7700633
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  • 14. Comparing histopathological classification with MYCN, 1p36 and 17q status detected by fluorescence in situ hybridisation from 14 untreated primary neuroblastomas in Singapore.
    Yong MH, Hwang WS, Knight LA, Fung W, Chan MY, Seow WT, Chui CH.
    Singapore Med J; 2009 Nov 16; 50(11):1090-4. PubMed ID: 19960166
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  • 16. 1;17 translocations and other chromosome 17 rearrangements in human primary neuroblastoma tumors and cell lines.
    Van Roy N, Laureys G, Cheng NC, Willem P, Opdenakker G, Versteeg R, Speleman F.
    Genes Chromosomes Cancer; 1994 Jun 16; 10(2):103-14. PubMed ID: 7520263
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  • 18. [The neuroblastoma, "enfant terrible" among pediatric tumors].
    Laureys G.
    Verh K Acad Geneeskd Belg; 2003 Jun 16; 65(1):5-23; discussion 23-8. PubMed ID: 12802894
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