These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

82 related articles for article (PubMed ID: 648191)

  • 1. Human somatic chromosome chains and rings. A preliminary note on end-to-end fusion.
    Dutrillaux B; Croquette MF; Viegas-Pequignot E; Aurias A; Coget J; Couturier J; Lejeune J
    Cytogenet Cell Genet; 1978; 20(1-6):70-7. PubMed ID: 648191
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The CREST syndrome variant of scleroderma in a mother-daughter pair.
    Mund DJ; Greenwald RA
    J Rheumatol; 1978; 5(3):307-10. PubMed ID: 748555
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial CRST syndrome with sicca complex.
    Frayha RA; Tabbara KF; Geha RS
    J Rheumatol; 1977; 4(1):53-8. PubMed ID: 886553
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. The relationship between sister chromatid exchanges and chromosome aberrations in Bloom's syndrome.
    Shiraishi Y; Sandberg AA
    Cytogenet Cell Genet; 1977; 18(1):13-23. PubMed ID: 871313
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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]  

  • 7. Mitotic recombination and segregation of satellites in Bloom's syndrome.
    Therman E; Otto PG; Shahidi NT
    Chromosoma; 1981; 82(5):627-36. PubMed ID: 7261713
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Thiberge-Weissenbach syndrome in a case of disseminated lupus erythematosus].
    HAINAUT J; MUSIN L; DRUEZ G
    Acta Clin Belg; 1960; 15():96-106. PubMed ID: 14398884
    [No Abstract]   [Full Text] [Related]  

  • 9. No increased chromosome breakage in three Bloom's syndrome heterozygotes.
    Kuhn EM; Therman E
    J Med Genet; 1979 Jun; 16(3):219-22. PubMed ID: 469900
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Chromosome aberrations and unscheduled DNA synthesis in X- and UV-irradiated lymphocytes from a boy with Bloom's syndrome and a man with xeroderma pigmentosum.
    Evans HJ; Adams AC; Clarkson JM; German J
    Cytogenet Cell Genet; 1978; 20(1-6):124-40. PubMed ID: 648171
    [No Abstract]   [Full Text] [Related]  

  • 11. [CRST syndrome (Thibierge-Weissenbach syndrome) in a patient with 13-year history of systemic scleroderma].
    Kierat J; Wojaczek W
    Wiad Lek; 1981 Apr; 34(7):599-602. PubMed ID: 7269606
    [No Abstract]   [Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exchange aberrations among 11 chromosomes of human lymphocytes induced by gamma-rays.
    Cafourková A; Luká ová E; Kozubek S; Kozubek M; Govorun RD; Koutná I; Bártová E; Skalníková M; Jirsová P; Paseková R; Krasavin EA
    Int J Radiat Biol; 2001 Apr; 77(4):419-29. PubMed ID: 11304436
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effects of chemicals on the frequency of sister chromatid exchanges and chromosome aberrations in normal and Bloom's syndrome lymphocytes.
    Shiraishi Y; Sandberg AA
    Cytobios; 1979; 26(102):91-108. PubMed ID: 121708
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The miR-146a rs2910164 C/G polymorphism is associated with telangiectasia in systemic sclerosis.
    Sakoguchi A; Jinnin M; Makino T; Kajihara I; Makino K; Honda N; Nakayama W; Inoue K; Fukushima S; Ihn H
    Clin Exp Dermatol; 2013 Jan; 38(1):99-100. PubMed ID: 23020128
    [No Abstract]   [Full Text] [Related]  

  • 16. Spontaneous and clastogen induced chromosomal breakage in scleroderma.
    Wolff DJ; Needleman BW; Wasserman SS; Schwartz S
    J Rheumatol; 1991 Jun; 18(6):837-40. PubMed ID: 1716681
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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]  

  • 18. 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]  

  • 19. 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; 38(3):145-50. PubMed ID: 8540685
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 5.