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Journal Abstract Search

270 related items for PubMed ID: 2323087

  • 1. 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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  • 2. Detection of the fragile X chromosome and other fragile sites.
    Webb GC.
    Clin Genet; 1985 May; 27(5):520-1. PubMed ID: 4006279
    [No Abstract] [Full Text] [Related]

  • 3. Increase in the incidence of the fragile site Xq27 in prometaphases.
    Barbi G, Steinbach P.
    Hum Genet; 1982 May; 61(1):82. PubMed ID: 6957373
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  • 5. [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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  • 7. Cytogenetic and physical mapping in the region of the X chromosome surrounding the fragile site.
    Nguyen C, Mattei MG, Rey JA, Baeteman MA, Mattei JF, Jordan BR.
    Am J Med Genet; 1988 Jul; 30(1-2):601-11. PubMed ID: 2902799
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  • 10. Frequency of tri- or multiradial configurations in fragile X identification.
    Jenkins EC, Duncan CJ, Krawczun MS, Berns LM, Sanz MM, Brown WT.
    Am J Med Genet; 1986 Jul; 23(1-2):531-5. PubMed ID: 2937304
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  • 11. 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 Jul; 1():345-54. PubMed ID: 3087195
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  • 13. Recombination and amplification of pyrimidine-rich sequences may be responsible for initiation and progression of the Xq27 fragile site: an hypothesis.
    Nussbaum RL, Airhart SD, Ledbetter DH.
    Am J Med Genet; 1986 Jul; 23(1-2):715-21. PubMed ID: 3456708
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  • 15. A marker X chromosome associated with nonspecific male mental retardation. The first South African cases.
    Venter PA, Gericke GS, Dawson B, Op't Hof J.
    S Afr Med J; 1981 Nov 21; 60(21):807-11. PubMed ID: 7302747
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  • 19. Constitutive fragile sites in fra(X) individuals.
    Jenkins EC, Lele KP, Krawczun MS, Gross AC, Duncan CJ, Brown WT.
    Am J Med Genet; 1988 Nov 21; 30(1-2):429-34. PubMed ID: 3052066
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  • 20. Characterisation of a new rare fragile site easily confused with the fragile X.
    Sutherland GR, Baker E.
    Hum Mol Genet; 1992 May 21; 1(2):111-3. PubMed ID: 1301146
    [Abstract] [Full Text] [Related]

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