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Journal Abstract Search

173 related items for PubMed ID: 4006279

  • 1.
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  • 2. The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X.
    Sutherland GR, Baker E.
    Clin Genet; 1990 Mar; 37(3):167-72. PubMed ID: 2323087
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  • 3. Increase in the incidence of the fragile site Xq27 in prometaphases.
    Barbi G, Steinbach P.
    Hum Genet; 1982 Mar; 61(1):82. PubMed ID: 6957373
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  • 5. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
    Voelckel MA, Philip N, Piquet C, Pellissier MC, Oberlé I, Birg F, Mattei MG, Mattei JF.
    Hum Genet; 1989 Mar; 81(4):353-7. PubMed ID: 2564838
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  • 6. Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.
    Blomquist HK, Gustavson KH, Holmgren G, Nordenson I, Pålsson-Stråe U.
    Clin Genet; 1983 Dec; 24(6):393-8. PubMed ID: 6652951
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  • 7. Constitutive fragile sites in fra(X) individuals.
    Jenkins EC, Lele KP, Krawczun MS, Gross AC, Duncan CJ, Brown WT.
    Am J Med Genet; 1988 Dec; 30(1-2):429-34. PubMed ID: 3052066
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  • 10. [Variations in the presence of a fragile site on X--fra(X)--according to cases and methods used].
    Crippa L, Delozier-Blanchet CD, Engel E.
    J Genet Hum; 1984 Jul; 32(3):193-7. PubMed ID: 6481341
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  • 11. [Fragile X syndrome].
    Lufei H.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Apr; 23(2):120-2. PubMed ID: 2202564
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  • 14. Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts.
    Kuwano A, Murano I, Kajii T.
    Hum Genet; 1990 May; 84(6):527-31. PubMed ID: 2338337
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  • 15. Detection of the fragile X chromosome and other fragile sites.
    Hecht F, Sutherland GR.
    Clin Genet; 1984 Oct; 26(4):301-3. PubMed ID: 6499245
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  • 16. Pulsed-field gradient-gel studies around the fragile site.
    Dobkin CS, Brown WT.
    Am J Med Genet; 1988 Oct; 30(1-2):593-600. PubMed ID: 2902798
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  • 17. Chromosome studies in 10 patients with the Rett syndrome.
    Moore JW, Tuck-Muller CM, Murphy M, Naidu S, Thomas GH.
    Am J Med Genet Suppl; 1986 Oct; 1():345-54. PubMed ID: 3087195
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  • 19. Expression of fragile site on the human X chromosome in somatic cell hybrids between human fragile X cells and thymidylate synthase-negative mouse mutant cells.
    Hori T, Ayusawa D, Glover TW, Seno T.
    Jpn J Cancer Res; 1985 Oct; 76(10):977-83. PubMed ID: 3935628
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