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Journal Abstract Search

199 related items for PubMed ID: 19682064

  • 1. Characterisation of hairy cell leukaemia by tiling resolution array-based comparative genome hybridisation: a series of 13 cases and review of the literature.
    Nordgren A, Corcoran M, Sääf A, Bremer A, Kluin-Nelemans HC, Schoumans J, Grandér D.
    Eur J Haematol; 2010 Jan 01; 84(1):17-25. PubMed ID: 19682064
    [Abstract] [Full Text] [Related]

  • 2. 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 01; 16(12):1450-8. PubMed ID: 18628790
    [Abstract] [Full Text] [Related]

  • 3. Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2.
    Schoumans J, Johansson B, Corcoran M, Kuchinskaya E, Golovleva I, Grandér D, Forestier E, Staaf J, Borg A, Gustafsson B, Blennow E, Nordgren A.
    Br J Haematol; 2006 Nov 01; 135(4):492-9. PubMed ID: 16999846
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  • 4. Genome-wide analysis of DNA copy number alterations and gene expression in gastric cancer.
    Tsukamoto Y, Uchida T, Karnan S, Noguchi T, Nguyen LT, Tanigawa M, Takeuchi I, Matsuura K, Hijiya N, Nakada C, Kishida T, Kawahara K, Ito H, Murakami K, Fujioka T, Seto M, Moriyama M.
    J Pathol; 2008 Dec 01; 216(4):471-82. PubMed ID: 18798223
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  • 6. A narrow deletion of 7q is common to HCL, and SMZL, but not CLL.
    Andersen CL, Gruszka-Westwood A, Østergaard M, Koch J, Jacobsen E, Kjeldsen E, Nielsen B.
    Eur J Haematol; 2004 Jun 01; 72(6):390-402. PubMed ID: 15128417
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  • 7. A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents.
    Knijnenburg J, Oberstein SA, Frei K, Lucas T, Gijsbers AC, Ruivenkamp CA, Tanke HJ, Szuhai K.
    J Med Genet; 2009 Jun 01; 46(6):412-7. PubMed ID: 19246478
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  • 9. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
    Kloth JN, Oosting J, van Wezel T, Szuhai K, Knijnenburg J, Gorter A, Kenter GG, Fleuren GJ, Jordanova ES.
    BMC Genomics; 2007 Feb 20; 8():53. PubMed ID: 17311676
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  • 11. Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH.
    Selvarajah S, Yoshimoto M, Ludkovski O, Park PC, Bayani J, Thorner P, Maire G, Squire JA, Zielenska M.
    Cytogenet Genome Res; 2008 Feb 20; 122(1):5-15. PubMed ID: 18931480
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  • 13. Determination of amplicon boundaries at 20q13.2 in tissue samples of human gastric adenocarcinomas by high-resolution microarray comparative genomic hybridization.
    Weiss MM, Snijders AM, Kuipers EJ, Ylstra B, Pinkel D, Meuwissen SG, van Diest PJ, Albertson DG, Meijer GA.
    J Pathol; 2003 Jul 20; 200(3):320-6. PubMed ID: 12845628
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  • 15. DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets.
    Mantripragada KK, Tapia-Páez I, Blennow E, Nilsson P, Wedell A, Dumanski JP.
    Int J Mol Med; 2004 Feb 20; 13(2):273-9. PubMed ID: 14719134
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  • 17. Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.
    Selzer RR, Richmond TA, Pofahl NJ, Green RD, Eis PS, Nair P, Brothman AR, Stallings RL.
    Genes Chromosomes Cancer; 2005 Nov 20; 44(3):305-19. PubMed ID: 16075461
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  • 19. Genomic changes detected by array CGH in human embryos with developmental defects.
    Rajcan-Separovic E, Qiao Y, Tyson C, Harvard C, Fawcett C, Kalousek D, Stephenson M, Philipp T.
    Mol Hum Reprod; 2010 Feb 20; 16(2):125-34. PubMed ID: 19778950
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  • 20. Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation.
    Koolen DA, Reardon W, Rosser EM, Lacombe D, Hurst JA, Law CJ, Bongers EM, van Ravenswaaij-Arts CM, Leisink MA, van Kessel AG, Veltman JA, de Vries BB.
    Eur J Hum Genet; 2005 Sep 20; 13(9):1019-24. PubMed ID: 15986041
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