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Journal Abstract Search

216 related items for PubMed ID: 6683244

  • 21. Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic association.
    Oberlé I, Boué J, Croquette MF, Voelckel MA, Mattei MG, Mandel JL.
    Am J Med Genet; ; 43(1-2):224-31. PubMed ID: 1605195
    [Abstract] [Full Text] [Related]

  • 22. Fragile sites on human chromosomes: description and clinical significance.
    Michels VV.
    Mayo Clin Proc; 1985 Oct; 60(10):690-6. PubMed ID: 3897734
    [Abstract] [Full Text] [Related]

  • 23. 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
    [Abstract] [Full Text] [Related]

  • 24. Fragile X expression and X inactivation. I. The expression of the fragile site at Xq27.3 is not suppressed on inactive X chromosomes separated from the active homologue.
    Wöhrle D, Fryns JP, Steinbach P.
    Hum Genet; 1990 Oct; 85(6):659-65. PubMed ID: 2227957
    [Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. Fragile X chromosome: consistent demonstration of fragile site in fibroblast cultures.
    Gardner AP, Howell RT, McDermott A.
    Lancet; 1982 Jan 09; 1(8263):101. PubMed ID: 6119461
    [No Abstract] [Full Text] [Related]

  • 27. The 'fragile' X chromosome in the Martin-Bell-Renpenning syndrome and in males with other forms of familial mental retardation.
    Proops R, Webb T.
    J Med Genet; 1981 Oct 09; 18(5):366-73. PubMed ID: 7328617
    [Abstract] [Full Text] [Related]

  • 28. Fragile X-linked mental retardation: the Martin-Bell syndrome.
    Richards BW, Sylvester PE, Brooker C.
    J Ment Defic Res; 1981 Dec 09; 25 Pt 4():253-6. PubMed ID: 7328634
    [Abstract] [Full Text] [Related]

  • 29. Manifestation of the fragile site Xq27 in fibroblasts. III. A method to demonstrate R-type replication patterns and the fragile site.
    Barbi G, Steinbach P, Wiedenmann A, Vogel W.
    Hum Genet; 1983 Dec 09; 65(1):76-8. PubMed ID: 6642510
    [Abstract] [Full Text] [Related]

  • 30. 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 Dec 09; 1():345-54. PubMed ID: 3087195
    [Abstract] [Full Text] [Related]

  • 31. 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 Dec 09; 66(2-3):225-9. PubMed ID: 6232199
    [Abstract] [Full Text] [Related]

  • 32. 5-Fluoro-2'-deoxyuridine induction of the fragile site on Xq28 associated with X linked mental retardation.
    Tommerup N, Poulsen H, Brøndum-Nielsen K.
    J Med Genet; 1981 Oct 09; 18(5):374-6. PubMed ID: 6460104
    [Abstract] [Full Text] [Related]

  • 33. Differential expression of fragile site Xq27 in cultured fibroblasts from hemizygotes and heterozygotes and its implications for prenatal diagnosis.
    Schmidt A, Passarge E.
    Am J Med Genet; 1986 Oct 09; 23(1-2):515-25. PubMed ID: 3953662
    [Abstract] [Full Text] [Related]

  • 34. 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 Oct 09; 29(1):59-61. PubMed ID: 3487280
    [Abstract] [Full Text] [Related]

  • 35. Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardation.
    Voelckel MA, Mattei MG, N'Guyen C, Philip N, Birg F, Mattei JF.
    Hum Genet; 1988 Dec 09; 80(4):375-8. PubMed ID: 2904402
    [Abstract] [Full Text] [Related]

  • 36. Further delineation of X-linked mental retardation.
    Herbst DS, Dunn HG, Dill FJ, Kalousek DK, Krywaniuk LW.
    Hum Genet; 1981 Dec 09; 58(4):366-72. PubMed ID: 6948768
    [Abstract] [Full Text] [Related]

  • 37. A variant of the fra(X) syndrome.
    Bühler EM, Hadziselimovic F, Pira U.
    Hum Genet; 1982 Dec 09; 61(3):273-5. PubMed ID: 6890944
    [Abstract] [Full Text] [Related]

  • 38. Fragile X expression studied by clonal analysis and somatic cell hybridization.
    Bryant EM, Martin GM, Hoehn H.
    Cytogenet Cell Genet; 1983 Dec 09; 35(3):223-5. PubMed ID: 6683146
    [Abstract] [Full Text] [Related]

  • 39. Fragile X expression and X inactivation. II. The fragile site at Xq27.3 has a basic function in the pathogenesis of fragile X-linked mental retardation.
    Wöhrle D, Steinbach P.
    Hum Genet; 1991 Aug 09; 87(4):421-4. PubMed ID: 1715307
    [Abstract] [Full Text] [Related]

  • 40. A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosome.
    Li SY, Tsai CC, Chou MY, Lin JK.
    Hum Genet; 1988 Aug 09; 79(4):292-6. PubMed ID: 2970423
    [Abstract] [Full Text] [Related]

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