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Journal Abstract Search

254 related items for PubMed ID: 7554365

  • 41. Superoxide dismutase activity and chromosome damage in cultured chromosome instability syndrome cells.
    Lee KH, Abe S, Yanabe Y, Matsuda I, Yoshida MC.
    Mutat Res; 1990 Jul; 244(3):251-6. PubMed ID: 2366819
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  • 43. [Use of a test exposing lymphocytes to mitomycin C in the diagnosis of Fanconi's anemia].
    Frías S, Carnevale A, del Castillo V.
    Rev Invest Clin; 1984 Jul; 36(3):219-24. PubMed ID: 6440252
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  • 44. Human genetic instability syndromes: single gene defects with increased risk of cancer.
    Digweed M.
    Toxicol Lett; 1993 Apr; 67(1-3):259-81. PubMed ID: 8451764
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  • 49. Acute lymphoblastic leukemia in a child with Fanconi's anaemia.
    Mushtaq N, Wali R, Fadoo Z, Saleem AF.
    J Coll Physicians Surg Pak; 2012 Jul; 22(7):458-60. PubMed ID: 22747869
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  • 54. The genetics of Fanconi's anaemia.
    Dokal I.
    Baillieres Best Pract Res Clin Haematol; 2000 Sep; 13(3):407-25. PubMed ID: 11030042
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  • 57. Cytogenetics of Bloom's syndrome.
    Kuhn EM, Therman E.
    Cancer Genet Cytogenet; 1986 May; 22(1):1-18. PubMed ID: 3513946
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  • 58. Fanconi's anemia: a clinico-hematological and cytogenetic study.
    Athale UH, Rao SR, Kadam PR, Gladstone B, Nair CN, Kurkure PA, Advani SH.
    Indian Pediatr; 1991 Sep; 28(9):1003-11. PubMed ID: 1802836
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  • 59. Fanconi's anaemia; chromosome breakage in a large African family.
    Meme JS, Greipenberg U, Kähkönen M.
    Hereditas; 1980 Sep; 93(2):255-60. PubMed ID: 7440242
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  • 60. Episphalosomic syndrome : a MCA syndrome ressembling Fanconi anemia, with increased baseline level of chromosome breaks but no hypersensivity to clastogens.
    Verloes A, Jamar M, Dideberg V, Herens C.
    Ann Genet; 2001 Sep; 44(2):59-62. PubMed ID: 11522241
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