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Journal Abstract Search

254 related items for PubMed ID: 7554365

  • 1. Retinoblastoma in association with the chromosome breakage syndromes Fanconi's anaemia and Bloom's syndrome: clinical and cytogenetic findings.
    Gibbons B, Scott D, Hungerford JL, Cheung KL, Harrison C, Attard-Montalto S, Evans M, Birch JM, Kingston JE.
    Clin Genet; 1995 Jun; 47(6):311-7. PubMed ID: 7554365
    [Abstract] [Full Text] [Related]

  • 2. [Chromosome instability syndromes].
    Germain D, Bernheim A.
    Sem Hop; 1983 Dec 01; 59(44):3065-79. PubMed ID: 6320395
    [Abstract] [Full Text] [Related]

  • 3. [Chromosome breakage syndrome and fragile X syndrome].
    Shiraishi Y.
    Nihon Rinsho; 1995 Nov 01; 53(11):2807-14. PubMed ID: 8538049
    [Abstract] [Full Text] [Related]

  • 4. 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 Nov 01; 61(4):342-56. PubMed ID: 7152519
    [Abstract] [Full Text] [Related]

  • 5. [Chromosome instability syndromes].
    Germain D, Bernheim A.
    Pathol Biol (Paris); 1982 Nov 01; 30(9):802-16. PubMed ID: 6760085
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  • 6. Clinical and cytogenetic diversity in Fanconi's anaemia.
    Duckworth-Rysiecki G, Hultén M, Mann J, Taylor AM.
    J Med Genet; 1984 Jun 01; 21(3):197-203. PubMed ID: 6431107
    [Abstract] [Full Text] [Related]

  • 7. [Bloom syndrome, constitutional and induced genetic instability in 2 cases from Argentina].
    Gorla NB, Bonduel MM, Lejarraga H, Sackman Muriel F, Larripa IB.
    Sangre (Barc); 1989 Dec 01; 34(6):475-80. PubMed ID: 2629124
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  • 9. Cytogenetic demonstration of a corrective factor in Bloom's syndrome.
    Rüdiger HW.
    IARC Sci Publ; 1982 Dec 01; (39):137-45. PubMed ID: 7152606
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  • 12. Genetic diseases associated with DNA and chromosomal instability.
    Lambert WC.
    Dermatol Clin; 1987 Jan 01; 5(1):85-108. PubMed ID: 3549081
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  • 13. Spontaneous chromosomal aberrations in Fanconi anaemia, ataxia telangiectasia fibroblast and Bloom's syndrome lymphoblastoid cell lines as detected by conventional cytogenetic analysis and fluorescence in situ hybridisation (FISH) technique.
    Sakamoto Hojo ET, van Diemen PC, Darroudi F, Natarajan AT.
    Mutat Res; 1995 Feb 01; 334(1):59-69. PubMed ID: 7799980
    [Abstract] [Full Text] [Related]

  • 14. Bloom's syndrome.
    Gretzula JC, Hevia O, Weber PJ.
    J Am Acad Dermatol; 1987 Sep 01; 17(3):479-88. PubMed ID: 3655026
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  • 15. Fanconi's aplastic anemia, analysis of 18 cases.
    Gözdaşoğlu S, Cavdar AO, Arcasoy A, Babacan E, Sanal O.
    Acta Haematol; 1980 Sep 01; 64(3):131-5. PubMed ID: 6778045
    [Abstract] [Full Text] [Related]

  • 16. Sister chromatid exchange evaluation as an aid to the diagnosis and exclusion of Fanconi's anaemia by induced chromosome damage analysis.
    Howell RT.
    J Med Genet; 1991 Jul 01; 28(7):468-71. PubMed ID: 1910092
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  • 17. Chromosome-breakage syndromes: different genes, different treatments, different cancers.
    German J.
    Basic Life Sci; 1980 Jul 01; 15():429-39. PubMed ID: 7011310
    [Abstract] [Full Text] [Related]

  • 18. The rate of sister chromatid exchanges parallel to spontaneous chromosome breakage in Fanconi's anemia and to trenimon-induced aberrations in human lymphocytes and fibroblasts.
    Hayashi K, Schmid W.
    Humangenetik; 1975 Sep 23; 29(3):201-6. PubMed ID: 1165100
    [Abstract] [Full Text] [Related]

  • 19. 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 23; 72(10):4066-70. PubMed ID: 1060089
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  • 20. Transformation of chromosome breakage syndrome fibroblasts by SV40 DNA transfection.
    Shaham M, Adler B, Chaganti RS.
    Cancer Genet Cytogenet; 1986 Feb 01; 20(1-2):137-47. PubMed ID: 3002603
    [Abstract] [Full Text] [Related]

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