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Journal Abstract Search

157 related items for PubMed ID: 2937304

  • 1. 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; 23(1-2):531-5. PubMed ID: 2937304
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  • 2. The fragile X(q27) form of X-linked mental retardation: FUdR as an inducing agent for fra(X)(q27) expression in lymphocytes, fibroblasts, and amniocytes.
    Brookwell R, Daniel A, Turner G, Fishburn J.
    Am J Med Genet; 1982 Oct; 13(2):139-48. PubMed ID: 6215863
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  • 3. Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome.
    Jenkins EC, Genovese MJ, Duncan CJ, Gu H, Stark-Houck SL, Lele K, Li SY, Krawczun MS.
    Am J Med Genet; 1982 Oct; 43(1-2):136-41. PubMed ID: 1605182
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  • 4. The combined effects of FUdR addition and methionine depletion on the X-chromosome fragile site.
    Glover TW, Howard-Peebles PN.
    Am J Hum Genet; 1983 Jan; 35(1):117-22. PubMed ID: 6218753
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  • 5. Fragile X expression increased by low cell-culture density.
    Krawczun MS, Lele KP, Jenkins EC, Brown WT.
    Am J Med Genet; 1986 Jan; 23(1-2):467-73. PubMed ID: 2937301
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  • 7. Variability of thymidylate synthase activity in whole blood cultures treated with FUdR.
    Sklower SL, Jenkins EC, Anderson ML, Chan CB, Brown WT.
    Am J Med Genet; 1986 Jan; 23(1-2):483-90. PubMed ID: 2937302
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  • 8. Fragile X expression in short-term whole blood cultures is affected by cell density.
    Krawczun MS, Jenkins EC, Brown WT, Silverman WP.
    Am J Med Genet; 1988 Jan; 30(1-2):435-42. PubMed ID: 2972206
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  • 9. Expression of the autosomal folate-sensitive fragile sites in ten kindreds with Martin-Bell syndrome.
    Ventruto V, Stabile M, Gentile G, de Tollis G, Colantuoni M, Sirone P, Perone L, Lonardo F, Della Monica M, Fiore M.
    Ann Genet; 1986 Jan; 29(1):59-61. PubMed ID: 3487280
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  • 12. Improved prenatal detection of fra(X)(q27.3): methods for prevention of false negatives in chorionic villus and amniotic fluid cell cultures.
    Jenkins EC, Krawczun MS, Stark-Houck SL, Duncan CJ, Kunaporn S, Gu H, Schwartz-Richstein C, Howard-Peebles PN, Gross A, Sherman SL.
    Am J Med Genet; 1991 Jan; 38(2-3):447-52. PubMed ID: 1826813
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  • 13. The effect of caffeine on fragile X expression.
    Abruzzo MA, Pettay D, Mayer M, Jacobs PA.
    Hum Genet; 1986 May; 73(1):20-2. PubMed ID: 2940164
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  • 14. The prenatal detection of the fragile X chromosome: review of recent experience.
    Jenkins EC, Brown WT, Wilson MG, Lin MS, Alfi OS, Wassman ER, Brooks J, Duncan CJ, Masia A, Krawczun MS.
    Am J Med Genet; 1986 May; 23(1-2):297-311. PubMed ID: 2937295
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  • 15. Dialyzed fetal bovine serum increases cytogenetic fragile X expression.
    Jenkins EC, Duncan CJ, Gu H, Genovese M, Krawczun MS.
    Am J Med Genet; 1986 May; 43(1-2):155-60. PubMed ID: 1534967
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  • 18. Cytogenetic investigations in mentally retarded and normal males from 14 families with the fragile site at Xq28. Results of folic acid treatment on fra(X) expression.
    Nielsen KB, Tommerup N.
    Hum Genet; 1984 May; 66(2-3):225-9. PubMed ID: 6232199
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  • 20. [Mental retardation linked to fragility of chromosome X: current knowledge].
    Mattei JF, Mattei MG, Auger M, Giraud F.
    J Genet Hum; 1984 Jul; 32(3):167-92. PubMed ID: 6237176
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