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Journal Abstract Search

164 related items for PubMed ID: 3177459

  • 1. Fragile X expression in normal and mentally retarded subjects: effect of treatment with an antifolic agent.
    Sanfilippo S, Ragusa RM, Scillato F, Ruggeri M, Neri G.
    Am J Med Genet; 1988; 30(1-2):369-76. PubMed ID: 3177459
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  • 2. Institutional screening for the fragile X syndrome.
    Hagerman R, Berry R, Jackson AW, Campbell J, Smith AC, McGavran L.
    Am J Dis Child; 1988 Nov; 142(11):1216-21. PubMed ID: 3177330
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  • 3. 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
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  • 4. 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 Jun; 23(1-2):581-7. PubMed ID: 3953668
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  • 8. 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 Jun; 23(1-2):589-95. PubMed ID: 3953669
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  • 9. A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndrome.
    Mayer M, Abruzzo MA, Jacobs PA, Yee SC.
    Hum Genet; 1985 Jun; 69(3):206-8. PubMed ID: 3980014
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  • 11. Fragile X syndrome in mildly mentally retarded children in a northern Swedish county. A prevalence study.
    Blomquist HK, Gustavson KH, Holmgren G, Nordenson I, Pålsson-Stråe U.
    Clin Genet; 1983 Dec; 24(6):393-8. PubMed ID: 6652951
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  • 12. Fragile X syndrome: a public health concern.
    Trusler S, Beatty-DeSana J.
    Am J Public Health; 1985 Jul; 75(7):771-2. PubMed ID: 4003653
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  • 13. Cytogenetic investigations in mentally retarded and normal males from 14 families with the fragile site at Xq28. Results of folic acid treatment on fra(X) expression.
    Nielsen KB, Tommerup N.
    Hum Genet; 1984 Jul; 66(2-3):225-9. PubMed ID: 6232199
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  • 14. Fra(X)(q27.2), the common fragile site, observed in only one of 760 cases studied for the fragile X syndrome.
    Jenkins EC, Genovese MJ, Duncan CJ, Gu H, Stark-Houck SL, Lele K, Li SY, Krawczun MS.
    Am J Med Genet; 1984 Jul; 43(1-2):136-41. PubMed ID: 1605182
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  • 15. [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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  • 17. Cytogenetic diagnosis of the fragile X syndrome: efficiency, utilization, and trends.
    Shapiro LR, Wilmot PL, Shapiro DA, Pettersen IM, Casamassima AC.
    Am J Med Genet; 1991 Feb; 38(2-3):408-10. PubMed ID: 2018082
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  • 18. The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986.
    Veenema H, Beverstock GC, de Koning T, Pearson PL, van de Kamp JJ.
    Clin Genet; 1988 Jun; 33(6):410-7. PubMed ID: 3168313
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  • 20. Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic association.
    Oberlé I, Boué J, Croquette MF, Voelckel MA, Mattei MG, Mandel JL.
    Am J Med Genet; 1988 Jun; 43(1-2):224-31. PubMed ID: 1605195
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