Discussion| Volume 17, ISSUE 5, P322, September 1995

The incidence of the fragile X syndrome in Japanese commentary on Nanba's paper

  • Yutaka Nakahori
    Corresponding author. Fax: (81) (3) 5802-2907.
    Department of Human Genetics, Graduate School of International Health, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113, Japan
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        • Verkerk A.J.M.H.
        • Pieretti M.
        • Sutcleffe J.
        • et al.
        Identification of a gene (FMR-1) containing a CGG repeat coincident with a break-point cluster region exhibiting length variation in fragile X syndrome.
        Cell. 1991; 65: 905-914
        • Nakahori Y.
        • Knight S.J.L.
        • Holland J.
        • et al.
        Molecular heterogeneity of the fragile X syndrome.
        Nucleic Acids Res. 1991; 19: 4355-4359
        • Arinami T.
        • Kondo I.
        • Nakajima S.
        Frequency of the fragile X syndrome in Japanese mentally retarded males.
        Hum Genet. 1986; 73: 309-312
        • Hofstee Y.
        • Arinami T.
        • Hamaguchi H.
        Comparison between the cytogenetic test for fragile X and the molecular analysis of the FMR-1 gene in Japanese mentally retarded individuals.
        Am J Med Genet. 1994; 51: 466-470
        • Knight S.J.L.
        • Flannery A.V.
        • Hirst M.C.
        • et al.
        Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.
        Cell. 1993; 74: 127-134