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Journal Abstract Search

155 related items for PubMed ID: 6499265

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  • 3. Fragile-X mental retardation syndrome transmitted through intellectually normal males: implications for genetic counseling.
    Young RS, Jaramillo C, McCombs JL, Moore CM, Jorgenson RJ.
    South Med J; 1986 Apr; 79(4):405-9. PubMed ID: 3704696
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  • 4. Normal male carriers in the fra(X) form of X-linked mental retardation (Martin-Bell syndrome).
    Froster-Iskenius U, McGillivray BC, Dill FJ, Hall JG, Herbst DS.
    Am J Med Genet; 1986 Apr; 23(1-2):619-31. PubMed ID: 3953672
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  • 7. [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; 32(3):199-207. PubMed ID: 6481342
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  • 10. Transmission of the marker X syndrome trait by unaffected males: conclusions from studies of large families.
    Froster-Iskenius U, Schulze A, Schwinger E.
    Hum Genet; 1984 Jul; 67(4):419-27. PubMed ID: 6593289
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  • 11. [Mental deficiency associated with a fragility of the X chromosome].
    Guitart Feliubadalo M, Artigas Pallarés J, Fuster Marqués C, Gabau Vila E, Lorente Hurtado I, Argemí Renom J.
    An Esp Pediatr; 1988 Nov; 29(5):377-81. PubMed ID: 3232895
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  • 12. Frequency of the fragile X syndrome in Japanese mentally retarded males.
    Arinami T, Kondo I, Nakajima S.
    Hum Genet; 1986 Aug; 73(4):309-12. PubMed ID: 3744362
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  • 13. [Familial mental retardation and the fragile X syndrome].
    Veenema H, Pelckmans AJ, Geraedts JP, Van Leeuwen I, Zvelebil N.
    Tijdschr Kindergeneeskd; 1984 Feb; 52(1):9-15. PubMed ID: 6585033
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  • 15. Dermatoglyphic findings in patients with fragile X-chromosome.
    Hirth L, Singh S, Schilling S, Müller E, Goedde HW.
    Clin Genet; 1985 Feb; 27(2):118-21. PubMed ID: 3978845
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  • 16. The female and the fragile X. A study of 144 obligate female carriers.
    Fryns JP.
    Am J Med Genet; 1986 Feb; 23(1-2):157-69. PubMed ID: 3953644
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  • 17. Fragile X syndrome: a common etiology of mental retardation.
    Rogers RC, Simensen RJ.
    Am J Ment Defic; 1987 Mar; 91(5):445-9. PubMed ID: 3565490
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  • 18. A deletion of 1.6 Kb proximal to the CGG repeat of the FMR1 gene causes fragile X-like psychological features.
    Wiegers AM, Curfs LM, Meijer H, Oostra B, Fryns JP.
    Genet Couns; 1994 Mar; 5(4):377-80. PubMed ID: 7888141
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  • 19. A community study of severe mental retardation in the West Midlands and the importance of the fragile X chromosome in its aetiology.
    Bundey S, Webb TP, Thake A, Todd J.
    J Med Genet; 1985 Aug; 22(4):258-66. PubMed ID: 4045951
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  • 20. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males.
    Soudek D, Partington MW, Lawson JS.
    Am J Med Genet; 1984 Jan; 17(1):241-52. PubMed ID: 6711598
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