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Journal Abstract Search

181 related items for PubMed ID: 7166308

  • 1. The cell cycle of lymphocytes in Fanconi anemia.
    Dutrillaux B, Aurias A, Dutrillaux AM, Buriot D, Prieur M.
    Hum Genet; 1982; 62(4):327-32. PubMed ID: 7166308
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  • 2. [Relationship of spontaneous chromosome instability and sister chromatid exchanges in Fanconi's anemia].
    Nazarenko SA, Burmakina IuE.
    Biull Eksp Biol Med; 1984 Sep; 98(9):334-6. PubMed ID: 6487791
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  • 3. Cytogenetic differentiation of Fanconi anemia, "idiopathic" aplastic anemia, and Fanconi anemia heterozygotes.
    Cervenka J, Hirsch BA.
    Am J Med Genet; 1983 Jun; 15(2):211-23. PubMed ID: 6410915
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  • 4. Fanconi's anemia--chromosome breakage studies in homozygotes and heterozygotes.
    Rosendorff J, Bernstein R.
    Cancer Genet Cytogenet; 1988 Jul 15; 33(2):175-83. PubMed ID: 3133104
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  • 7. Frequency and distribution of sister-chromatid exchanges in a case of Fanconi's anemia.
    Sperling K, Wegner RD, Riehm H, Obe G.
    Humangenetik; 1975 Jul 15; 27(3):227-30. PubMed ID: 50275
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  • 8. Fanconi's anemia lymphocytes: effect of caffeine, adenosine and niacinamide during G2 prophase.
    Pincheira J, Bravo M, López-Sáez JF.
    Mutat Res; 1988 May 15; 199(1):159-65. PubMed ID: 2966295
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  • 9. Failure of diepoxybutane to enhance sister chromatid exchange levels in Fanconi's anemia patients and heterozygotes.
    Porfirio B, Dallapiccola B, Mokini V, Alimena G, Gandini E.
    Hum Genet; 1983 May 15; 63(2):117-20. PubMed ID: 6840755
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  • 10. The effect of aphidicolin on Fanconi's anemia lymphocyte chromosomes.
    Porfirio B, Dallapiccola B, Gandini E.
    Mutat Res; 1985 Dec 15; 144(4):257-63. PubMed ID: 3934533
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  • 11. Prevention of chromosomal breakage in Fanconi's anemia by cocultivation with normal cells.
    Nordenson I, Björksten B, Lundh B.
    Hum Genet; 1980 Dec 15; 56(2):169-71. PubMed ID: 7450773
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  • 13. Flow cytometric characterization of the response of Fanconi's anemia cells to mitomycin C treatment.
    Kaiser TN, Lojewski A, Dougherty C, Juergens L, Sahar E, Latt SA.
    Cytometry; 1982 Mar 15; 2(5):291-7. PubMed ID: 6804195
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  • 16. Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia.
    Latt SA, Stetten G, Juergens LA, Buchanan GR, Gerald PS.
    Proc Natl Acad Sci U S A; 1975 Oct 15; 72(10):4066-70. PubMed ID: 1060089
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  • 17. [Fanconi's anemia: in vitro tests for the individualization of heterozygotes].
    Farulla A, Monaco E, Corrao CR, Cardoni F, Simonazzi S, Dallapiccola B.
    G Ital Med Lav; 1986 Oct 15; 8(3-4):133-8. PubMed ID: 3330716
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  • 18. Cytogenetic and flow cytometric studies of cells from patients with Fanconi's anemia.
    Latt SA, Kaiser TN, Lojewski A, Dougherty C, Juergens L, Brefach S, Sahar E, Gustashaw K, Schreck RR, Powers M, Lalande M.
    Cytogenet Cell Genet; 1982 Oct 15; 33(1-2):133-8. PubMed ID: 7116934
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  • 20. Position of chromosomes in the human interphase nucleus. An analysis of nonhomologous chromatid translocations in lymphocyte cultures after Trenimon treatment and from patients with Fanconi's anemia and Bloom's syndrome.
    Hager HD, Schroeder-Kurth TM, Vogel F.
    Hum Genet; 1982 Oct 15; 61(4):342-56. PubMed ID: 7152519
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