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PUBMED FOR HANDHELDS

Journal Abstract Search


124 related items for PubMed ID: 6878899

  • 41. Esterase D and hereditary retinoblastoma.
    Burde RM.
    Am J Ophthalmol; 1984 Jun; 97(6):779-82. PubMed ID: 6731544
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  • 42. [Increased sister-chromatid exchanges in fibroblasts from a del(13)-retinoblastoma patient (author's transl)].
    Turleau C, Cabanis MO, de Grouchy J.
    Ann Genet; 1980 Jun; 23(3):169-70. PubMed ID: 6968533
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  • 43. [Hereditary tumors and chromosome aberrations with special reference to retinoblastoma].
    Sasaki MS.
    Gan To Kagaku Ryoho; 1986 Mar; 13(3 Pt 2):645-51. PubMed ID: 3963835
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  • 48. Toward clinical microcytogenetics: the aniridia and the retinoblastoma stories.
    de Grouchy J.
    Prog Clin Biol Res; 1982 Mar; 103 Pt B():359-67. PubMed ID: 6298811
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  • 52. Cytogenetic analysis of retinoblastoma: evidence for multifocal origin and in vivo gene amplification.
    Chaum E, Ellsworth RM, Abramson DH, Haik BG, Kitchin FD, Chaganti RS.
    Cytogenet Cell Genet; 1984 Mar; 38(2):82-91. PubMed ID: 6467991
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  • 53. Retinoblastoma. A model of hereditary fragile chromosomal regions.
    Hashem N, Khalifa S.
    Hum Hered; 1975 Mar; 25(1):35-49. PubMed ID: 1150293
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  • 54. Further observations on a 13qXp translocation associated with retinoblastoma.
    Nichols WW, Miller RC, Sobel M, Hoffman E, Sparkes RS, Mohandas T, Veomett I, Davis JR.
    Am J Ophthalmol; 1980 May; 89(5):621-7. PubMed ID: 7189644
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  • 55. Cytogenetics in retinoblastomas.
    Rao KS, Rao CR, Radhakrishna G.
    Indian J Ophthalmol; 1975 Oct; 23(3):23-5. PubMed ID: 1236311
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  • 56. Frequency of 13q abnormalities among 203 patients with retinoblastoma.
    Bunin GR, Emanuel BS, Meadows AT, Buckley JD, Woods WG, Hammond GD.
    J Natl Cancer Inst; 1989 Mar 01; 81(5):370-4. PubMed ID: 2915374
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