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Journal Abstract Search

147 related items for PubMed ID: 3295640

  • 1. Retinoblastoma, chromosome abnormalities and oncogene expression.
    Gilbert F, Potluri VR, Short MP, Kau CL, Lalatta F.
    Ophthalmic Paediatr Genet; 1987 Mar; 8(1):3-10. PubMed ID: 3295640
    [Abstract] [Full Text] [Related]

  • 2. Chromosomal abnormalities in human retinoblastoma. A review.
    Potluri VR, Helson L, Ellsworth RM, Reid T, Gilbert F.
    Cancer; 1986 Aug 01; 58(3):663-71. PubMed ID: 3524791
    [Abstract] [Full Text] [Related]

  • 3. Nonrandom chromosomal changes in retinoblastomas.
    Pogosianz HE, Kuznetsova LE.
    Arch Geschwulstforsch; 1986 Aug 01; 56(2):135-43. PubMed ID: 3707294
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  • 4. Complete or partial homozygosity of chromosome 13 in primary retinoblastoma.
    Benedict WF, Srivatsan ES, Mark C, Banerjee A, Sparkes RS, Murphree AL.
    Cancer Res; 1987 Aug 01; 47(15):4189-91. PubMed ID: 2886215
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  • 5. Simultaneous existence of double minute chromosomes and a homogeneously staining region in a retinoblastoma cell line (Y79) and amplification of N-myc at HSR.
    Inazawa J, Abe T, Inoue K, Nishigaki H, Horiike S, Taniwaki M, Misawa S, Takino T.
    Cancer Genet Cytogenet; 1989 Jan 01; 37(1):133-7. PubMed ID: 2917328
    [Abstract] [Full Text] [Related]

  • 6. Constitutional karyotypes in retinoblastoma.
    Turleau C, De Grouchy J.
    Ophthalmic Paediatr Genet; 1987 Mar 01; 8(1):11-7. PubMed ID: 3295639
    [Abstract] [Full Text] [Related]

  • 7. Cytogenetics in retinoblastomas.
    Rao KS, Rao CR, Radhakrishna G.
    Indian J Ophthalmol; 1975 Oct 01; 23(3):23-5. PubMed ID: 1236311
    [No Abstract] [Full Text] [Related]

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  • 9. Retinoblastoma with 13q- chromosomal deletion associated with maternal paracentric inversion of 13q.
    Sparkes RS, Muller H, Klisak I.
    Science; 1979 Mar 09; 203(4384):1027-9. PubMed ID: 424728
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  • 10. Homogeneously staining regions and tumorigenicity.
    Gilbert F, Balaban G, Brangman D, Herrmann N, Lister A.
    Int J Cancer; 1983 Jun 15; 31(6):765-8. PubMed ID: 6862685
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  • 15. Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes.
    Balaban G, Gilbert F, Nichols W, Meadows AT, Shields J.
    Cancer Genet Cytogenet; 1982 Jul 15; 6(3):213-21. PubMed ID: 7116319
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  • 16. Retinoblastoma and partial deletion of the long arm of chromosome 13.
    Howard RO, Warburton D, Breg WR, Miller OJ, McKeown J, Rubin SP.
    Trans Am Ophthalmol Soc; 1978 Jul 15; 76():172-83. PubMed ID: 754371
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  • 17. [Molecular genetics and retinoblastoma].
    Sahel J.
    J Fr Ophtalmol; 1988 Jul 15; 11(2):133-5. PubMed ID: 3171092
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  • 18. Familial pericentric inversion of chromosome 11 in a child with sporadic unilateral retinoblastoma.
    Ohnishi Y, Shigeto M, Ishibashi T, Hirata J.
    Ophthalmic Paediatr Genet; 1990 Dec 15; 11(4):281-5. PubMed ID: 2096356
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  • 20. 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 15; 179(2):102-11. PubMed ID: 18036396
    [Abstract] [Full Text] [Related]

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