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Journal Abstract Search

169 related items for PubMed ID: 18253027

  • 21. Tissue microarray-based screening for chromosomal breakpoints affecting the T-cell receptor gene loci in mature T-cell lymphomas.
    Leich E, Haralambieva E, Zettl A, Chott A, Rüdiger T, Höller S, Müller-Hermelink HK, Ott G, Rosenwald A.
    J Pathol; 2007 Sep; 213(1):99-105. PubMed ID: 17582237
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  • 22. Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH.
    Lindstrand A, Schoumans J, Gustavsson P, Hanemaaijer N, Malmgren H, Blennow E.
    Clin Genet; 2010 Jun; 77(6):552-62. PubMed ID: 20236111
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  • 26. Micro-array analyses decipher exceptional complex familial chromosomal rearrangement.
    Fauth C, Gribble SM, Porter KM, Codina-Pascual M, Ng BL, Kraus J, Uhrig S, Leifheit J, Haaf T, Fiegler H, Carter NP, Speicher MR.
    Hum Genet; 2006 Mar; 119(1-2):145-53. PubMed ID: 16395598
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  • 27. Two genetic pathways, t(1;10) and amplification of 3p11-12, in myxoinflammatory fibroblastic sarcoma, haemosiderotic fibrolipomatous tumour, and morphologically similar lesions.
    Hallor KH, Sciot R, Staaf J, Heidenblad M, Rydholm A, Bauer HC, Aström K, Domanski HA, Meis JM, Kindblom LG, Panagopoulos I, Mandahl N, Mertens F.
    J Pathol; 2009 Apr; 217(5):716-27. PubMed ID: 19199331
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  • 29. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.
    Espinosa AB, Mackintosh C, Maíllo A, Gutierrez L, Sousa P, Merino M, Ortiz J, de Alava E, Orfao A, Tabernero MD.
    Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790
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  • 31. Mapping of constitutional translocation breakpoints in renal cell cancer patients: identification of KCNIP4 as a candidate gene.
    Bonne A, Vreede L, Kuiper RP, Bodmer D, Jansen C, Eleveld M, van Erp F, Arkesteijn G, Hoogerbrugge N, van Ravenswaaij C, Schoenmakers EF, Geurts van Kessel A.
    Cancer Genet Cytogenet; 2007 Nov; 179(1):11-8. PubMed ID: 17981209
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  • 33. 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; 179(2):102-11. PubMed ID: 18036396
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  • 34. A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects.
    Spitz F, Montavon T, Monso-Hinard C, Morris M, Ventruto ML, Antonarakis S, Ventruto V, Duboule D.
    Genomics; 2002 Apr; 79(4):493-8. PubMed ID: 11944980
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  • 35. Trisomy 2 due to a 3:1 segregation in an abortion studied by QF-PCR and CGH.
    Lorda-Sánchez I, Diego-Alvarez D, Ayuso C, de Alba MR, Trujillo MJ, Ramos C.
    Prenat Diagn; 2005 Oct; 25(10):934-8. PubMed ID: 16088866
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  • 36. Localization of centromeric breaks in head and neck squamous cell carcinoma.
    Martínez JG, Pérez-Escuredo J, Llorente JL, Suárez C, Hermsen MA.
    Cancer Genet; 2012 Dec; 205(12):622-9. PubMed ID: 23164608
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  • 40. Amplification of the ABCB1 region accompanied by a short sequence of 200bp from chromosome 2 in lung cancer cells.
    Kitada K, Yamasaki T, Aikawa S.
    Cancer Genet Cytogenet; 2009 Oct; 194(1):4-11. PubMed ID: 19737648
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