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Journal Abstract Search

149 related items for PubMed ID: 8844099

  • 1. FRAXE mutation analysis in three Spanish families.
    Carbonell P, López I, Gabarrón J, Bernabé MJ, Lucas JM, Guitart M, Gabau E, Glover G.
    Am J Med Genet; 1996 Aug 09; 64(2):434-40. PubMed ID: 8844099
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  • 2. The influence of expanded unmethylated alleles for FRAXA/FRAXE loci in the intellectual performance among Brazilian mentally impaired males.
    Barros Santos C, Gonçalves Pimentel MM.
    Int J Mol Med; 2003 Sep 09; 12(3):385-9. PubMed ID: 12883656
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  • 3. Molecular characterization of FRAXE-positive subjects with mental impairement in two unrelated Italian families.
    Russo S, Selicorni A, Bedeschi MF, Natacci F, Viziello P, Fortuna R, Pagani G, Dalprà L, Larizza L.
    Am J Med Genet; 1998 Jan 23; 75(3):304-8. PubMed ID: 9475603
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  • 6. FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population.
    Syrrou M, Georgiou I, Grigoriadou M, Petersen MB, Kitsiou S, Pagoulatos G, Patsalis PC.
    Genet Epidemiol; 1998 Jan 23; 15(1):103-9. PubMed ID: 9523214
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  • 7. Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: incidence, genetic variation, and stability.
    Patsalis PC, Sismani C, Hettinger JA, Boumba I, Georgiou I, Stylianidou G, Anastasiadou V, Koukoulli R, Pagoulatos G, Syrrou M.
    Am J Med Genet; 1999 May 28; 84(3):184-90. PubMed ID: 10331587
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  • 10. Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.
    Parrish JE, Oostra BA, Verkerk AJ, Richards CS, Reynolds J, Spikes AS, Shaffer LG, Nelson DL.
    Nat Genet; 1994 Nov 28; 8(3):229-35. PubMed ID: 7874164
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  • 12. A survey of fragile X syndrome in a sample from Spanish Basque country.
    Arrieta I, Criado B, Martinez B, Telez M, Nuñez T, Peñagarikano O, Ortega B, Lostao CM.
    Ann Genet; 1999 Nov 28; 42(4):197-201. PubMed ID: 10674158
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  • 13. Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males.
    Biancalana V, Taine L, Bouix JC, Finck S, Chauvin A, De Verneuil H, Knight SJ, Stoll C, Lacombe D, Mandel JL.
    Am J Hum Genet; 1996 Oct 28; 59(4):847-54. PubMed ID: 8808600
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  • 16. FRAXA locus in fragile X diagnosis: family studies, prenatal diagnosis, and diagnosis of sporadic cases of mental retardation.
    von Koskull H, Gahmberg N, Salonen R, Salo A, Peippo M.
    Am J Med Genet; 1994 Jul 15; 51(4):486-9. PubMed ID: 7943025
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  • 18. Clinical, cytogenetic, and molecular analysis of three families with FRAXE.
    Barnicoat AJ, Wang Q, Turk J, Green E, Mathew CG, Flynn G, Buckle V, Hirst M, Davies K, Bobrow M.
    J Med Genet; 1997 Jan 15; 34(1):13-7. PubMed ID: 9032643
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