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Journal Abstract Search

102 related items for PubMed ID: 2740689

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  • 6. [Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics].
    Benítez J, Fernández E, Ramos C, Nunes V, del Río E, Baiget M.
    Rev Clin Esp; 1989 Apr; 184(7):364-6. PubMed ID: 2570446
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  • 7. Diagnostic molecular genetics of the fragile X.
    Sutherland GR, Mulley JC.
    Clin Genet; 1990 Jan; 37(1):2-11. PubMed ID: 1967989
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  • 8. [The molecular genetics of the fragile X syndrome. Its molecular diagnosis by DNA probes].
    Giné R, Espinás ML, Antich J, Carballo M.
    Med Clin (Barc); 1992 Feb 01; 98(4):121-4. PubMed ID: 1552760
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  • 9. Genetics and expression of the fragile X syndrome.
    Brown WT, Jenkins EC, Gross AC, Chan CB, Wisniewski K, Cohen IL, Miezejeski CM.
    Ups J Med Sci Suppl; 1987 Feb 01; 44():137-54. PubMed ID: 2895523
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  • 10. Further evidence for genetic heterogeneity in the fragile X syndrome.
    Brown WT, Jenkins EC, Gross AC, Chan CB, Krawczun MS, Duncan CJ, Sklower SL, Fisch GS.
    Hum Genet; 1987 Apr 01; 75(4):311-21. PubMed ID: 2883105
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  • 12. [Mental retardation and fragile X chromosome. Clinical and cytogenetic study of 3 families].
    Gilgenkrantz S, Boué J, Grégoire MJ, Tejada I.
    J Genet Hum; 1984 Jul 01; 32(3):199-207. PubMed ID: 6481342
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  • 13. [Fragile X chromosome and autistic mental retardation. Apropos of 23 cases].
    Bénézech M, Noel B, Noel L, Bourgeois M.
    Ann Med Psychol (Paris); 1983 Nov 01; 141(9):1006-11. PubMed ID: 6666917
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  • 15. [The adult mentally handicapped in psychiatry. Etiologic study with research on the fragile X chromosome].
    Ferauge M.
    Acta Psychiatr Belg; 1986 Nov 01; 86(3):287-96. PubMed ID: 3751650
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  • 16. DNA linkage studies in the fragile X syndrome suggest genetic heterogeneity.
    Brown WT, Gross AC, Chan CB, Jenkins EC.
    Am J Med Genet; 1986 Nov 01; 23(1-2):643-64. PubMed ID: 3006490
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  • 19. Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq.
    Buchanan JA, Buckton KE, Gosden CM, Newton MS, Clayton JF, Christie S, Hastie N.
    Hum Genet; 1987 Jun 01; 76(2):165-72. PubMed ID: 3038730
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