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253 related items for PubMed ID: 12203774

  • 1. Localization of the 17q breakpoint of a constitutional 1;17 translocation in a patient with neuroblastoma within a 25-kb segment located between the ACCN1 and TLK2 genes and near the distal breakpoints of two microdeletions in neurofibromatosis type 1 patients.
    Van Roy N, Vandesompele J, Berx G, Staes K, Van Gele M, De Smet E, De Paepe A, Laureys G, van der Drift P, Versteeg R, Van Roy F, Speleman F.
    Genes Chromosomes Cancer; 2002 Oct; 35(2):113-20. PubMed ID: 12203774
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  • 2. [Identification of the breakpoint-flanking markers on chromosomes 1 and 17 of a constitutional translocation T(1;17)(P36;Q12-21) in a patient with neuroblastoma].
    Laureys GG.
    Verh K Acad Geneeskd Belg; 1995 Oct; 57(5):389-422. PubMed ID: 8571670
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  • 5. Identification of the breakpoints at 1p36.2 and 3p21.3 in an AML(M3) patient who had t(1;3)(p36.2;p21.3) at the third relapse.
    Tri NK, Xinh PT, Nagao H, Izumi T, Ozawa K, Toyoda A, Hattori M, Sakaki Y, Tokunaga K, Sato Y.
    Genes Chromosomes Cancer; 2002 Dec; 35(4):365-7. PubMed ID: 12378531
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  • 7. [The neuroblastoma, "enfant terrible" among pediatric tumors].
    Laureys G.
    Verh K Acad Geneeskd Belg; 2003 Dec; 65(1):5-23; discussion 23-8. PubMed ID: 12802894
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  • 9. 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; 34(4):428-36. PubMed ID: 12112532
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  • 10. Smallest region of overlapping deletion in 1p36 in human neuroblastoma: a 1 Mbp cosmid and PAC contig.
    Bauer A, Savelyeva L, Claas A, Praml C, Berthold F, Schwab M.
    Genes Chromosomes Cancer; 2001 Jul; 31(3):228-39. PubMed ID: 11391793
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  • 11. Three chromosomal rearrangements in neuroblastoma cluster within a 300-kb region on 1p36.1.
    Spieker N, Beitsma M, Van Sluis P, Chan A, Caron H, Versteeg R.
    Genes Chromosomes Cancer; 2001 Jun; 31(2):172-81. PubMed ID: 11319804
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  • 12. Breakpoint characterization of der(9) deletions in chronic myeloid leukemia patients.
    Storlazzi CT, Specchia G, Anelli L, Albano F, Pastore D, Zagaria A, Rocchi M, Liso V.
    Genes Chromosomes Cancer; 2002 Nov; 35(3):271-6. PubMed ID: 12353269
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  • 14. 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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  • 15. Genomic and functional map of the chromosome 14 t(12;14) breakpoint cluster region in uterine leiomyoma.
    Lynch RA, Piper M, Bankier A, Bhugra B, Surti U, Liu J, Buckler A, Dear PH, Menon AG.
    Genomics; 1998 Aug 15; 52(1):17-26. PubMed ID: 9740667
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  • 16. Molecular characterization of a genetically unstable region containing the SMS critical area and a breakpoint cluster for human PNETs.
    Wilgenbus KK, Seranski P, Brown A, Leuchs B, Mincheva A, Lichter P, Poustka A.
    Genomics; 1997 May 15; 42(1):1-10. PubMed ID: 9177769
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  • 17. Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma.
    Lastowska M, Van Roy N, Bown N, Speleman F, Roberts P, Lunec J, Strachan T, Pearson AD, Jackson MS.
    Med Pediatr Oncol; 2001 Jan 15; 36(1):20-3. PubMed ID: 11464884
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  • 18. A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes.
    Kuhlenbäumer G, Schirmacher A, Meuleman J, Tissir F, Del-Favero J, Stögbauer F, Young P, Ringelstein B, Van Broeckhoven C, Timmerman V.
    Genomics; 1999 Dec 01; 62(2):242-50. PubMed ID: 10610718
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  • 19. A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet.
    Kondoh S, Sugawara H, Harada N, Matsumoto N, Ohashi H, Sato M, Kantaputra PN, Ogino T, Tomita H, Ohta T, Kishino T, Fukushima Y, Niikawa N, Yoshiura K.
    J Hum Genet; 2002 Dec 01; 47(3):136-9. PubMed ID: 11954550
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  • 20. Construction of a detailed physical and transcript map of the candidate region for Russell-Silver syndrome on chromosome 17q23-q24.
    Dörr S, Midro AT, Färber C, Giannakudis J, Hansmann I.
    Genomics; 2001 Jan 15; 71(2):174-81. PubMed ID: 11161811
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