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Journal Abstract Search

127 related items for PubMed ID: 8071962

  • 1. Isolation and characterisation of a panel of cosmids which allows unequivocal identification of chromosome deletions involving the RB1 gene using fluorescence in situ hybridisation.
    Cowell JK, Jaju R, Kempski H.
    J Med Genet; 1994 Apr; 31(4):334-7. PubMed ID: 8071962
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  • 10. Chromosome abnormalities and RB1 gene deletions in chronic lymphocytic leukemia.
    Juliusson G, Gahrton G, Einhorn S, Liu Y, Oscier DG, Chapman R.
    Blood; 1993 Sep 15; 82(6):1938-9. PubMed ID: 8400245
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  • 11. [Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients].
    Munier F, Balmer A, von Moos C, Pescia G, Gailloud C, van Melle G, Thonney F, Gaide AC, Allaz MJ, Rutz HP.
    Klin Monbl Augenheilkd; 1991 May 15; 198(5):419-24. PubMed ID: 1886375
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  • 12. Chromosome 13 instability and esterase D expression in an osteosarcoma cell line.
    Hovig E, Winberg JO, Fodstad O, Brøgger A, Gedde-Dahl T.
    Cancer Genet Cytogenet; 1987 Feb 15; 24(2):327-34. PubMed ID: 2878716
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  • 16. The RB1 gene is the target of chromosome 13 deletions in malignant fibrous histiocytoma.
    Chibon F, Mairal A, Fréneaux P, Terrier P, Coindre JM, Sastre X, Aurias A.
    Cancer Res; 2000 Nov 15; 60(22):6339-45. PubMed ID: 11103795
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  • 17. The decrease of catalase or esterase D activity in patients with microdeletions of 11p or 13q does not increase their radiosensitivity.
    Sabatier L, Hoffschir F, al Achkar WA, Turleau C, de Grouchy J, Dutrillaux B.
    Ann Genet; 1989 Nov 15; 32(3):144-8. PubMed ID: 2554783
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  • 20. De novo 13q partial duplication identified by cytogenetic, biochemical and molecular approaches.
    Schwartz S, Harris M, Ehrenpreis R, Zaslav A, Raffel LJ, Schwartz MF, Lieber E, Cohen MM.
    Clin Genet; 1991 Dec 15; 40(6):417-22. PubMed ID: 1778004
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