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153 related items for PubMed ID: 10862045

  • 1. Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses.
    Mairal A, Pinglier E, Gilbert E, Peter M, Validire P, Desjardins L, Doz F, Aurias A, Couturier J.
    Genes Chromosomes Cancer; 2000 Aug; 28(4):370-9. PubMed ID: 10862045
    [Abstract] [Full Text] [Related]

  • 2. Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization.
    Zielinski B, Gratias S, Toedt G, Mendrzyk F, Stange DE, Radlwimmer B, Lohmann DR, Lichter P.
    Genes Chromosomes Cancer; 2005 Jul; 43(3):294-301. PubMed ID: 15834944
    [Abstract] [Full Text] [Related]

  • 3. Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome.
    Lillington DM, Kingston JE, Coen PG, Price E, Hungerford J, Domizio P, Young BD, Onadim Z.
    Genes Chromosomes Cancer; 2003 Feb; 36(2):121-8. PubMed ID: 12508240
    [Abstract] [Full Text] [Related]

  • 4. Efficacy of high-resolution comparative genomic hybridization (HR-CGH) in detection of chromosomal abnormalities in children with acute leukaemia.
    Vranova V, Mentzlova D, Oltova A, Linkova V, Zezulkova D, Filkova H, Mendelova D, Sterba J, Kuglik P.
    Neoplasma; 2008 Feb; 55(1):23-30. PubMed ID: 18190236
    [Abstract] [Full Text] [Related]

  • 5. 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; 18(3):162-9. PubMed ID: 9071568
    [Abstract] [Full Text] [Related]

  • 6. Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
    Schoumans J, Ruivenkamp C, Holmberg E, Kyllerman M, Anderlid BM, Nordenskjöld M.
    J Med Genet; 2005 Sep; 42(9):699-705. PubMed ID: 16141005
    [Abstract] [Full Text] [Related]

  • 7. High-resolution mapping of amplifications and deletions in pediatric osteosarcoma by use of CGH analysis of cDNA microarrays.
    Squire JA, Pei J, Marrano P, Beheshti B, Bayani J, Lim G, Moldovan L, Zielenska M.
    Genes Chromosomes Cancer; 2003 Nov; 38(3):215-25. PubMed ID: 14506695
    [Abstract] [Full Text] [Related]

  • 8. Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.
    Ness GO, Lybaek H, Houge G.
    Am J Med Genet; 2002 Nov 22; 113(2):125-36. PubMed ID: 12407702
    [Abstract] [Full Text] [Related]

  • 9. Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.
    Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G.
    Ann Genet; 1998 Nov 22; 41(3):133-40. PubMed ID: 9833066
    [Abstract] [Full Text] [Related]

  • 10. Genetic profiling of colorectal cancer liver metastases by combined comparative genomic hybridization and G-banding analysis.
    Diep CB, Parada LA, Teixeira MR, Eknaes M, Nesland JM, Johansson B, Lothe RA.
    Genes Chromosomes Cancer; 2003 Feb 22; 36(2):189-97. PubMed ID: 12508247
    [Abstract] [Full Text] [Related]

  • 11. Genetic diagnosis by comparative genomic hybridization in adult de novo acute myelocytic leukemia.
    Casas S, Aventín A, Fuentes F, Vallespí T, Granada I, Carrió A, Angel Martínez-Climent J, Solé F, Teixidó M, Bernués M, Duarte J, Maria Hernández J, Brunet S, Dolors Coll M, Sierra J.
    Cancer Genet Cytogenet; 2004 Aug 22; 153(1):16-25. PubMed ID: 15325089
    [Abstract] [Full Text] [Related]

  • 12. Identification of a novel homozygous deletion region at 6q23.1 in medulloblastomas using high-resolution array comparative genomic hybridization analysis.
    Hui AB, Takano H, Lo KW, Kuo WL, Lam CN, Tong CY, Chang Q, Gray JW, Ng HK.
    Clin Cancer Res; 2005 Jul 01; 11(13):4707-16. PubMed ID: 16000565
    [Abstract] [Full Text] [Related]

  • 13. Genotypic analysis of esophageal squamous cell carcinoma by molecular cytogenetics and real-time quantitative polymerase chain reaction.
    Yen CC, Chen YJ, Lu KH, Hsia JY, Chen JT, Hu CP, Chen PM, Liu JH, Chiou TJ, Wang WS, Yang MH, Chao TC, Lin CH.
    Int J Oncol; 2003 Oct 01; 23(4):871-81. PubMed ID: 12963965
    [Abstract] [Full Text] [Related]

  • 14. Comparative genomic hybridization (CGH) analysis of neuroblastomas--an important methodological approach in paediatric tumour pathology.
    Brinkschmidt C, Christiansen H, Terpe HJ, Simon R, Boecker W, Lampert F, Stoerkel S.
    J Pathol; 1997 Apr 01; 181(4):394-400. PubMed ID: 9196436
    [Abstract] [Full Text] [Related]

  • 15. Nonrandom chromosomal changes in retinoblastomas.
    Pogosianz HE, Kuznetsova LE.
    Arch Geschwulstforsch; 1986 Apr 01; 56(2):135-43. PubMed ID: 3707294
    [Abstract] [Full Text] [Related]

  • 16. Whole genome amplification for CGH analysis: Linker-adapter PCR as the method of choice for difficult and limited samples.
    Pirker C, Raidl M, Steiner E, Elbling L, Holzmann K, Spiegl-Kreinecker S, Aubele M, Grasl-Kraupp B, Marosi C, Micksche M, Berger W.
    Cytometry A; 2004 Sep 01; 61(1):26-34. PubMed ID: 15351986
    [Abstract] [Full Text] [Related]

  • 17. Mapping of chromosomal gains and losses in primitive neuroectodermal tumors by comparative genomic hybridization.
    Schütz BR, Scheurlen W, Krauss J, du Manoir S, Joos S, Bentz M, Lichter P.
    Genes Chromosomes Cancer; 1996 Jul 01; 16(3):196-203. PubMed ID: 8814453
    [Abstract] [Full Text] [Related]

  • 18. Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma.
    Lau CC, Harris CP, Lu XY, Perlaky L, Gogineni S, Chintagumpala M, Hicks J, Johnson ME, Davino NA, Huvos AG, Meyers PA, Healy JH, Gorlick R, Rao PH.
    Genes Chromosomes Cancer; 2004 Jan 01; 39(1):11-21. PubMed ID: 14603437
    [Abstract] [Full Text] [Related]

  • 19. Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization.
    Naus NC, van Drunen E, de Klein A, Luyten GP, Paridaens DA, Alers JC, Ksander BR, Beverloo HB, Slater RM.
    Genes Chromosomes Cancer; 2001 Mar 01; 30(3):267-73. PubMed ID: 11170284
    [Abstract] [Full Text] [Related]

  • 20. Constitutional genomic instability, chromosome aberrations in tumor cells and retinoblastoma.
    Amare Kadam PS, Ghule P, Jose J, Bamne M, Kurkure P, Banavali S, Sarin R, Advani S.
    Cancer Genet Cytogenet; 2004 Apr 01; 150(1):33-43. PubMed ID: 15041221
    [Abstract] [Full Text] [Related]

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