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Journal Abstract Search

141 related items for PubMed ID: 3177477

  • 1. The fragile X in Sicily: an epidemiological survey.
    Neri G, Sanfilippo S, Pavone L, Mollica F, Barberi I, Giuffrè L, Romano C, Mattina T, Cammarata M, Ragusa MG.
    Am J Med Genet; 1988; 30(1-2):665-72. PubMed ID: 3177477
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  • 2. Fragile X mental retardation: prevalence in a group of institutionalized patients in Italy and description of a novel EEG pattern.
    Sanfilippo S, Ragusa RM, Musumeci S, Neri G.
    Am J Med Genet; 1986; 23(1-2):589-95. PubMed ID: 3953669
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  • 3. 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(4):735-9. PubMed ID: 3239562
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  • 4. Frequency of the fragile X syndrome in institutionalized mentally retarded females in Japan.
    Arinami T, Kondo I, Nakajima S, Hamaguchi H.
    Hum Genet; 1987 Aug; 76(4):344-7. PubMed ID: 3610153
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  • 5. X-linked mental retardation. I. Martin-Bell syndrome (report of 18 families).
    Rocchi M, Archidiacono N, Filippi G.
    J Genet Hum; 1987 Dec; 35(5):351-79. PubMed ID: 3437265
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  • 6. Prevalence of the fragile-X syndrome in mentally retarded boys in a Swedish county.
    Gustavson KH, Blomquist HK, Holmgren G.
    Am J Med Genet; 1986 Dec; 23(1-2):581-7. PubMed ID: 3953668
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  • 7. Is there a fragile(X) negative Martin-Bell syndrome?
    Thode A, Laing S, Partington MW, Turner G.
    Am J Med Genet; 1988 Dec; 30(1-2):459-71. PubMed ID: 3052069
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  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Population incidence and segregation ratios in the Martin-Bell syndrome.
    Webb TP, Bundey SE, Thake AI, Todd J.
    Am J Med Genet; 1986 Aug; 23(1-2):573-80. PubMed ID: 3953667
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  • 10. Fragile X syndrome: incidence, clinical and cytogenetic findings in the black and white populations of South Carolina.
    Schwartz CE, Phelan MC, Pulliam LH, Wilkes G, Vanner LV, Albiez KL, Potts WA, Rogers RC, Schroer RJ, Saul RA.
    Am J Med Genet; 1988 Aug; 30(1-2):641-54. PubMed ID: 3177476
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  • 11. Fragile site X chromosomes in mentally retarded boys.
    Moon HR, Moon SY.
    J Korean Med Sci; 1993 Jun; 8(3):192-6. PubMed ID: 8240748
    [Abstract] [Full Text] [Related]

  • 12. A clinical, cytogenetic and familial study of 307 mentally retarded, institutionalized, adult male patients with special interest for fra(X) negative X-linked mental retardation.
    Haspeslagh M, Fryns JP, Holvoet M, Collen G, Dierck G, Baeke J, van den Berghe H.
    Clin Genet; 1991 Jun; 39(6):434-41. PubMed ID: 1863991
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  • 14. Expression of the fragile site Xq27 in fibroblasts. II. Evidence for negative and positive clones from heterozygous females and possible relationship between frequency and phenotype.
    Steinbach P, Barbi G, Baur S, Vogel W.
    Hum Genet; 1983 Jun; 64(3):279-82. PubMed ID: 6885072
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  • 15. The fragile X syndrome (Martin-Bell syndrome). Clinical and cytogenetic findings in 16 prepubertal boys and in 4 of their 5 families.
    Schinzel A, Largo RH.
    Helv Paediatr Acta; 1985 Jul; 40(2-3):133-52. PubMed ID: 3843245
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  • 19. Infantile autism: an occasional manifestation of fragile (X) mental retardation.
    McGillivray BC, Herbst DS, Dill FJ, Sandercock HJ, Tischler B.
    Am J Med Genet; 1986 Jul; 23(1-2):353-8. PubMed ID: 3953653
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