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Journal Abstract Search

119 related items for PubMed ID: 2937750

  • 21. Retinoblastoma. A model of hereditary fragile chromosomal regions.
    Hashem N, Khalifa S.
    Hum Hered; 1975; 25(1):35-49. PubMed ID: 1150293
    [Abstract] [Full Text] [Related]

  • 22. Retinoblastoma: a model of oncogenesis.
    Gallie BL, Phillips RA.
    Ophthalmology; 1984 Jun; 91(6):666-72. PubMed ID: 6462624
    [Abstract] [Full Text] [Related]

  • 23. A decreasing tendency for cytogenetic abnormality in peripheral lymphocytes of retinoblastoma patients with 13q14 deletion mosaicism.
    Motegi T, Minoda K.
    Hum Genet; 1984 Jun; 66(2-3):186-9. PubMed ID: 6714979
    [Abstract] [Full Text] [Related]

  • 24. Human retinoblastoma susceptibility gene: genomic organization and analysis of heterozygous intragenic deletion mutants.
    Bookstein R, Lee EY, To H, Young LJ, Sery TW, Hayes RC, Friedmann T, Lee WH.
    Proc Natl Acad Sci U S A; 1988 Apr; 85(7):2210-4. PubMed ID: 2895471
    [Abstract] [Full Text] [Related]

  • 25. Immortalization of fibroblasts from two patients with hereditary retinoblastoma.
    Banerjee A, Srivatsan E, Hashimoto T, Takahashi R, Xu HJ, Hu SX, Benedict WF.
    Anticancer Res; 1992 Apr; 12(5):1347-54. PubMed ID: 1359829
    [Abstract] [Full Text] [Related]

  • 26. Genetics of retinoblastoma.
    Vogel F.
    Hum Genet; 1979 Nov 01; 52(1):1-54. PubMed ID: 393614
    [Abstract] [Full Text] [Related]

  • 27. Deletion of chromosome region 13q14 is transmissible and does not always predispose to retinoblastoma.
    Cowell JK, Rutland P, Hungerford J, Jay M.
    Hum Genet; 1988 Sep 01; 80(1):43-5. PubMed ID: 2901396
    [Abstract] [Full Text] [Related]

  • 28. Characteristics of a cell line established from a patient with multiple osteosarcoma, appearing 13 years after treatment for bilateral retinoblastoma.
    Fodstad O, Brøgger A, Bruland O, Solheim OP, Nesland JM, Pihl A.
    Int J Cancer; 1986 Jul 15; 38(1):33-40. PubMed ID: 3459716
    [Abstract] [Full Text] [Related]

  • 29. Loss of heterozygosity on chromosome 13 and its association with delayed growth of retinoblastoma.
    Kato MV, Ishizaki K, Ejima Y, Kaneko A, Tanooka H, Sasaki MS.
    Int J Cancer; 1993 Jul 30; 54(6):922-6. PubMed ID: 8335400
    [Abstract] [Full Text] [Related]

  • 30. An in vitro investigation of x-ray sensitivity in fibroblasts from patients with retinoblastoma.
    Weichselbaum R, Albert DM, Cassady JR, Little JB.
    Invest Ophthalmol Vis Sci; 1983 Jul 30; 24(7):958-61. PubMed ID: 6862797
    [Abstract] [Full Text] [Related]

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  • 34. X-ray, UV and chemical mutagen sensitivities of skin fibroblasts from patients with familial and chromosome 13q- retinoblastomas.
    Fujiwara Y, Miyazaki N, Kano Y, Takahashi T, Kaneko A.
    J Radiat Res; 1981 Dec 30; 22(4):472-6. PubMed ID: 7338842
    [No Abstract] [Full Text] [Related]

  • 35. Application of PCR amplification of DNA from paraffin embedded tissue sections to linkage analysis in familial retinoblastoma.
    Onadim Z, Cowell JK.
    J Med Genet; 1991 May 30; 28(5):312-6. PubMed ID: 1865468
    [Abstract] [Full Text] [Related]

  • 36. Genetic origin of mutations predisposing to retinoblastoma.
    Cavenee WK, Hansen MF, Nordenskjold M, Kock E, Maumenee I, Squire JA, Phillips RA, Gallie BL.
    Science; 1985 Apr 26; 228(4698):501-3. PubMed ID: 3983638
    [Abstract] [Full Text] [Related]

  • 37. The sometime suppressor gene RB 1.
    Rosen P.
    Med Hypotheses; 1992 Jul 26; 38(3):259-60. PubMed ID: 1513285
    [No Abstract] [Full Text] [Related]

  • 38. Lymphocyte chromosome survey in 42 patients with retinoblastoma: effort to detect 13q14 deletion mosaicism.
    Motegi T.
    Hum Genet; 1981 Jul 26; 58(2):168-73. PubMed ID: 7287000
    [Abstract] [Full Text] [Related]

  • 39. Recent advances in the understanding of retinoblastoma.
    Hungerford JL.
    Trans Ophthalmol Soc U K (1962); 1985 Jul 26; 104 ( Pt 8)():832-5. PubMed ID: 3868875
    [Abstract] [Full Text] [Related]

  • 40. Family studies on the chromosomal location of the retinoblastoma gene (Rb-1).
    Morten J, Harnden DG, Bundey S.
    J Med Genet; 1982 Apr 26; 19(2):120-4. PubMed ID: 6951997
    [Abstract] [Full Text] [Related]

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