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Journal Abstract Search

97 related items for PubMed ID: 6140531

  • 1. Institutional prevalence of fragile X syndrome.
    Kinnell HG, Banu SP.
    Lancet; 1983 Dec 17; 2(8364):1427. PubMed ID: 6140531
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  • 9. Population based prenatal screening for the fragile X syndrome.
    Palomaki GE.
    J Med Screen; 1994 Jan 17; 1(1):65-72. PubMed ID: 8790488
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  • 10. Population incidence and segregation ratios in the Martin-Bell syndrome.
    Webb TP, Bundey SE, Thake AI, Todd J.
    Am J Med Genet; 1986 Jan 17; 23(1-2):573-80. PubMed ID: 3953667
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  • 11. The frequency of the fragile X chromosome among schoolchildren in Coventry.
    Webb TP, Bundey S, Thake A, Todd J.
    J Med Genet; 1986 Oct 17; 23(5):396-9. PubMed ID: 3783615
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  • 12. Fragile X syndrome is less common than previously estimated.
    Morton JE, Bundey S, Webb TP, MacDonald F, Rindl PM, Bullock S.
    J Med Genet; 1997 Jan 17; 34(1):1-5. PubMed ID: 9032640
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  • 15. Fragile site X chromosomes and X-linked mental retardation in severely retarded boys in a northern Swedish county. A prevalence study.
    Blomquist HK, Gustavson KH, Holmgren G, Nordenson I, Sweins A.
    Clin Genet; 1982 Mar 17; 21(3):209-14. PubMed ID: 7201364
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  • 16. Fragile X in a survey of 75 autistic males.
    Watson MS, Leckman JF, Annex B, Breg WR, Boles D, Volkmar FR, Cohen DJ, Carter C.
    N Engl J Med; 1984 May 31; 310(22):1462. PubMed ID: 6717529
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  • 20. Martin-Bell syndrome in Greece, with report of another 47,XXY fragile X patient.
    Mavrou A, Syrrou M, Tsenghi C, Agelakis M, Youroukos S, Metaxotou C.
    Am J Med Genet; 1988 Dec 31; 31(4):735-9. PubMed ID: 3239562
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