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Journal Abstract Search

129 related items for PubMed ID: 3036341

  • 1. Common cytogenetic findings in primary breast cancer.
    Ferti-Passantonopoulou AD, Panani AD.
    Cancer Genet Cytogenet; 1987 Aug; 27(2):289-98. PubMed ID: 3036341
    [Abstract] [Full Text] [Related]

  • 2. A cytogenetic study of male breast cancer.
    Mitchell EL.
    Cancer Genet Cytogenet; 1990 Jul 01; 47(1):107-12. PubMed ID: 2162731
    [Abstract] [Full Text] [Related]

  • 3. Cytogenetic features of twenty-six primary breast cancers.
    Hainsworth PJ, Raphael KL, Stillwell RG, Bennett RC, Garson OM.
    Cancer Genet Cytogenet; 1991 Jun 01; 53(2):205-18. PubMed ID: 1648438
    [Abstract] [Full Text] [Related]

  • 4. Cytogenetic analysis in human breast carcinoma. II. Seven cases in the triploid/tetraploid range investigated using direct preparations.
    Hill SM, Rodgers CS, Hultén MA.
    Cancer Genet Cytogenet; 1987 Jan 01; 24(1):45-62. PubMed ID: 3024810
    [Abstract] [Full Text] [Related]

  • 5. Cytogenetic analysis in a case of cancer of the male breast.
    Rodgers CS, Hill SM, Hultén MA.
    Cancer Genet Cytogenet; 1985 Feb 01; 15(1-2):113-7. PubMed ID: 2981608
    [Abstract] [Full Text] [Related]

  • 6. Chromosome analysis of in situ breast cancer.
    Nielsen KV, Blichert-Toft M, Andersen J.
    Acta Oncol; 1989 Feb 01; 28(6):919-22. PubMed ID: 2558694
    [Abstract] [Full Text] [Related]

  • 7. Cytogenetic analysis in human breast carcinoma. I. Nine cases in the diploid range investigated using direct preparations.
    Rodgers CS, Hill SM, Hultén MA.
    Cancer Genet Cytogenet; 1984 Oct 01; 13(2):95-119. PubMed ID: 6090007
    [Abstract] [Full Text] [Related]

  • 8. Trisomy 8 as a recurrent clonal abnormality in breast cancer?
    Bullerdiek J, Leuschner E, Taquia E, Bonk U, Bartnitzke S.
    Cancer Genet Cytogenet; 1993 Jan 01; 65(1):64-7. PubMed ID: 8381713
    [Abstract] [Full Text] [Related]

  • 9. Preferential involvement of chromosome 1q in a primary breast carcinoma.
    Kovacs G.
    Cancer Genet Cytogenet; 1981 Mar 01; 3(2):125-9. PubMed ID: 7272991
    [Abstract] [Full Text] [Related]

  • 10. Chromosome changes of in situ carcinomas in the female breast.
    Nielsen KV, Andersen JA, Blichert-Toft M.
    Eur J Surg Oncol; 1987 Jun 01; 13(3):225-9. PubMed ID: 3036604
    [Abstract] [Full Text] [Related]

  • 11. Chromosome analysis of 20 breast carcinomas: cytogenetic multiclonality and karyotypic-pathologic correlations.
    Pandis N, Heim S, Bardi G, Idvall I, Mandahl N, Mitelman F.
    Genes Chromosomes Cancer; 1993 Jan 01; 6(1):51-7. PubMed ID: 7680222
    [Abstract] [Full Text] [Related]

  • 12. Complete cytogenetic characterization of the human breast cancer cell line MA11 combining G-banding, comparative genomic hybridization, multicolor fluorescence in situ hybridization, RxFISH, and chromosome-specific painting.
    Micci F, Teixeira MR, Heim S.
    Cancer Genet Cytogenet; 2001 Nov 01; 131(1):25-30. PubMed ID: 11734314
    [Abstract] [Full Text] [Related]

  • 13. Cancer of the breast in twin sisters.
    Shmoulevitch P, Robinson E.
    Oncology; 1974 Nov 01; 30(3):192-6. PubMed ID: 4376589
    [No Abstract] [Full Text] [Related]

  • 14. Preferential involvement of 11q23-24 and 11p15 in breast cancer.
    Ferti-Passantonopoulou A, Panani AD, Raptis S.
    Cancer Genet Cytogenet; 1991 Feb 01; 51(2):183-8. PubMed ID: 1993303
    [Abstract] [Full Text] [Related]

  • 15. Accumulation of genetic alterations and progression of primary breast cancer.
    Sato T, Akiyama F, Sakamoto G, Kasumi F, Nakamura Y.
    Cancer Res; 1991 Nov 01; 51(21):5794-9. PubMed ID: 1682035
    [Abstract] [Full Text] [Related]

  • 16. Cytogenetic subtype involving chromosome 13 in lipoma. Report of three cases.
    Sreekantaiah C, Berger CS, Karakousis CP, Rao U, Leong SP, Sandberg AA.
    Cancer Genet Cytogenet; 1989 Jun 01; 39(2):281-8. PubMed ID: 2752378
    [Abstract] [Full Text] [Related]

  • 17. Interstitial deletion of the short arm of chromosome 3 as a primary chromosome abnormality in carcinomas of the breast.
    Pandis N, Jin Y, Limon J, Bardi G, Idvall I, Mandahl N, Mitelman F, Heim S.
    Genes Chromosomes Cancer; 1993 Mar 01; 6(3):151-5. PubMed ID: 7682099
    [Abstract] [Full Text] [Related]

  • 18. Familial fragile site found at the cancer breakpoint (1)(q32). Inducibility by distamycin A, concomitance with fragile (16)(q22).
    Shabtai F, Hart J, Klar D, Halbrecht I.
    Hum Genet; 1986 Jul 01; 73(3):232-4. PubMed ID: 3460959
    [Abstract] [Full Text] [Related]

  • 19. Molecular cytogenetic analysis of breast cancer: a combined multicolor fluorescence in situ hybridization and G-banding study of uncultured tumor cells.
    Ferti AD, Stamouli MJ, Panani AD, Raptis SA, Young BD.
    Cancer Genet Cytogenet; 2004 Feb 01; 149(1):28-37. PubMed ID: 15104280
    [Abstract] [Full Text] [Related]

  • 20. Cytogenetic effects of radiotherapy. Breakpoint distribution in induced chromosome aberrations.
    Barrios L, Miró R, Caballín MR, Fuster C, Guedea F, Subias A, Egozcue J.
    Cancer Genet Cytogenet; 1989 Aug 01; 41(1):61-70. PubMed ID: 2766252
    [Abstract] [Full Text] [Related]

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