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Journal Abstract Search

84 related items for PubMed ID: 5125548

  • 1. Chromosomal breakage in diffuse scleroderma. A study of 27 patients.
    Emerit I, Housset E, de Grouchy J, Camus JP.
    Rev Eur Etud Clin Biol; 1971; 16(7):684-94. PubMed ID: 5125548
    [No Abstract] [Full Text] [Related]

  • 2. Chromosomal alterations in scleroderma.
    Constantin M, Leucuţia M, Purice S.
    Med Interne; 1987; 25(4):245-9. PubMed ID: 3423700
    [Abstract] [Full Text] [Related]

  • 3. [Generalized scleroderma and chromosome breakage. Demonstration of a breaking factor in patients serum].
    Emerit I, Levy A, Housset E.
    Ann Genet; 1973 Jun; 16(2):135-8. PubMed ID: 4541907
    [No Abstract] [Full Text] [Related]

  • 4. Chromosomal breakage and scleroderma: studies in family members.
    Emerit I, Housset E, Feingold J.
    J Lab Clin Med; 1976 Jul; 88(1):81-6. PubMed ID: 932535
    [Abstract] [Full Text] [Related]

  • 5. Breakage factor in systemic sclerosis and protector effect of L-cysteine.
    Emerit I, Levy A, Housset E.
    Humangenetik; 1974 Jul; 25(3):221-6. PubMed ID: 4448453
    [No Abstract] [Full Text] [Related]

  • 6. A cytogenetic analysis of twenty cases of systemic scleroderma.
    Romani F, Viguie F, Siffroi JP, Fiessenger JN.
    Ann Genet; 1986 Jul; 29(4):240-5. PubMed ID: 3495226
    [Abstract] [Full Text] [Related]

  • 7. [Chromosome abnormalities in systemic scleroderma].
    Emerit I, Camus JP.
    Rev Rhum Mal Osteoartic; 1972 Nov; 39(11):731-4. PubMed ID: 4654971
    [No Abstract] [Full Text] [Related]

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  • 9. Chromosomal breakage in systemic sclerosis and related disorders.
    Emerit I.
    Dermatologica; 1976 Nov; 153(3):145-56. PubMed ID: 14037
    [Abstract] [Full Text] [Related]

  • 10. Chromosome changes in lymphocytes of patients with scleroderma.
    Casalone R, Granata P, Minelli E, Righi R, Meroni E, Mazzola D, Sammarelli G, Baratelli E, Broggini M.
    Ann Genet; 1995 Nov; 38(3):145-50. PubMed ID: 8540685
    [Abstract] [Full Text] [Related]

  • 11. [Cytogenetic aspects of diffuse scleroderma : structural anomalies and sister chromatid exchanges (author's transl)].
    Huet-Warembourg E, Legoff D, Jalbert H, Sele B, Amblard P, Reymond JL, Jalbert P, Pison H.
    Ann Genet; 1982 Nov; 25(1):32-5. PubMed ID: 6979297
    [Abstract] [Full Text] [Related]

  • 12. [Chromosome aberrations caused by diagnostic ultrasonics on human lymphocytes in culture].
    Bugnon C, Cottin Y, Kraehenbuhl J, Weill F.
    J Radiol Electrol Med Nucl; 1972 Oct; 53(10):750-5. PubMed ID: 4640547
    [No Abstract] [Full Text] [Related]

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  • 14. Chromosome abnormalities from cyclophosphamide therapy in rheumatoid arthritis and progressive systemic sclerosis (scleroderma).
    Tolchin SF, Winkelstein A, Rodnan GP, Pan SF, Nankin HR.
    Arthritis Rheum; 1974 Oct; 17(4):375-82. PubMed ID: 4851019
    [No Abstract] [Full Text] [Related]

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  • 17. [Etiology and pathogenesis of systemic scleroderma].
    Guseva NG.
    Revmatologiia (Mosk); 1983 Oct; (2):3-10. PubMed ID: 6312527
    [No Abstract] [Full Text] [Related]

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  • 19. [Familial scleroderma with Sjogren's syndrome and lymphocyte and chromosome abnormalities].
    Camus JP, Emerit I, Reinert P, Guillien P, Crouzet J, Fourot J.
    Ann Med Interne (Paris); 1970 Feb; 121(2):149-61. PubMed ID: 5491196
    [No Abstract] [Full Text] [Related]

  • 20. [Chromatid structural changes of chromosomal origin as a result of mitotic crossing over between sister chromatids in ring chromosomes].
    Nemtseva LS, Dubinin NP.
    Dokl Akad Nauk SSSR; 1969 Jun 11; 186(5):1185-8. PubMed ID: 5397312
    [No Abstract] [Full Text] [Related]

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