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Journal Abstract Search

119 related items for PubMed ID: 2937750

  • 41. Loss of heterozygosity on chromosome 17 and mutation of the p53 gene in retinoblastoma.
    Kato MV, Shimizu T, Ishizaki K, Kaneko A, Yandell DW, Toguchida J, Sasaki MS.
    Cancer Lett; 1996 Aug 23; 106(1):75-82. PubMed ID: 8827049
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  • 42. [Hereditary tumors and chromosome aberrations with special reference to retinoblastoma].
    Sasaki MS.
    Gan To Kagaku Ryoho; 1986 Mar 23; 13(3 Pt 2):645-51. PubMed ID: 3963835
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  • 43. Multistage and multifactorial carcinogenesis in hereditary tumours, with special reference to retinoblastoma.
    Matsunaga E.
    IARC Sci Publ; 1984 Mar 23; (56):373-83. PubMed ID: 6536602
    [No Abstract] [Full Text] [Related]

  • 44. Fibroblasts from patients with inherited predisposition to retinoblastoma exhibit normal sensitivity to the mutagenic effects of ionizing radiation.
    Wang Y, Parks WC, Wigle JC, Maher VM, McCormick JJ.
    Mutat Res; 1986 Oct 23; 175(2):107-14. PubMed ID: 3762576
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  • 45. Incidence and significance of a deletion of chromosome band 13q14 in patients with retinoblastoma and in their families.
    Liberfarb RM, Bustos T, Miller WA, Sang D.
    Ophthalmology; 1984 Dec 23; 91(12):1695-9. PubMed ID: 6521998
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  • 46. Nonrandom chromosomal changes in retinoblastomas.
    Pogosianz HE, Kuznetsova LE.
    Arch Geschwulstforsch; 1986 Dec 23; 56(2):135-43. PubMed ID: 3707294
    [Abstract] [Full Text] [Related]

  • 47. Deletions of the esterase D locus from a survey of 200 retinoblastoma patients.
    Cowell JK, Rutland P, Jay M, Hungerford J.
    Hum Genet; 1986 Feb 23; 72(2):164-7. PubMed ID: 3943870
    [Abstract] [Full Text] [Related]

  • 48. Bilateral retinoblastoma associated with 13q-mosaicism. Possible manifestation of a germinal mutation.
    Ribeiro MC, Andrade JA, Erwenne CM, Brunoni D.
    Cancer Genet Cytogenet; 1988 Jun 23; 32(2):169-75. PubMed ID: 3365680
    [Abstract] [Full Text] [Related]

  • 49. Chromosome 13 restriction fragment length polymorphisms.
    Dryja TP, Rapaport JM, Weichselbaum R, Bruns GA.
    Hum Genet; 1984 Jun 23; 65(4):320-4. PubMed ID: 6319270
    [Abstract] [Full Text] [Related]

  • 50. Molecular detection and differentiation of deletions in band 13q14 in human retinoblastoma.
    Lalande M, Donlon T, Petersen RA, Liberfarb R, Manter S, Latt SA.
    Cancer Genet Cytogenet; 1986 Oct 23; 23(2):151-7. PubMed ID: 3756834
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  • 56. In vitro studies of fibroblasts from patients with retinoblastoma.
    Nove J, Weichselbaum RR, Nichols WW, Albert DM, Little JB.
    Int Ophthalmol Clin; 1980 Oct 23; 20(2):211-22. PubMed ID: 6995388
    [No Abstract] [Full Text] [Related]

  • 57. High rate of detection of 13q14 deletion mosaicism among retinoblastoma patients (using more extensive methods).
    Motegi T.
    Hum Genet; 1982 Oct 23; 61(2):95-7. PubMed ID: 7129450
    [No Abstract] [Full Text] [Related]

  • 58. [A case of bilateral retinoblastoma with monosomy 13 (q12 leads to 114) (author's transl)].
    Walbaum R, François P, Farriaux JP, Woillez M.
    Hum Genet; 1978 Oct 31; 44(2):219-26. PubMed ID: 730167
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