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Journal Abstract Search

170 related items for PubMed ID: 12210320

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  • 2. Haplotype study of intermediate-length alleles at the fragile X (FMR1) gene: ATL1, FMRb, and microsatellite haplotypes differ from those found in common-size FMR1 alleles.
    Curlis Y, Zhang C, Holden JJ, Loesch PK, Mitchell RJ.
    Hum Biol; 2005 Feb; 77(1):137-51. PubMed ID: 16114822
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  • 3. Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia.
    Larsen LA, Vuust J, Nystad M, Evseeva I, Van Ghelue M, Tranebjaerg L.
    Eur J Hum Genet; 2001 Sep; 9(9):724-7. PubMed ID: 11571563
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  • 4. FRAXAC1 and DXS548 polymorphisms in the Chinese population.
    Poon PM, Pang CP, Chen QL, Zhong N, Lai KY, Lau CH, Wong CK, Brown WT.
    Am J Med Genet; 1999 May 28; 84(3):208-13. PubMed ID: 10331593
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  • 5. AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations.
    Angeli CB, Capelli LP, Auricchio MT, Leal-Mesquita ER, Ribeiro-dos-Santos AK, Ferrari I, Oliveira SF, Klautau-Guimarães Mde N, Vianna-Morgante AM, Mingroni-Netto RC.
    Am J Med Genet A; 2005 Jan 15; 132A(2):210-4. PubMed ID: 15551304
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  • 6. Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population.
    Jara L, Aspillaga M, Avendaño I, Obreque V, Blanco R, Valenzuela CY.
    Am J Med Genet; 1998 Jan 23; 75(3):277-82. PubMed ID: 9475597
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  • 8. Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.
    Crawford DC, Schwartz CE, Meadows KL, Newman JL, Taft LF, Gunter C, Brown WT, Carpenter NJ, Howard-Peebles PN, Monaghan KG, Nolin SL, Reiss AL, Feldman GL, Rohlfs EM, Warren ST, Sherman SL.
    Am J Hum Genet; 2000 Feb 23; 66(2):480-93. PubMed ID: 10677308
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  • 10. Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population.
    Zhong N, Liu X, Gou S, Houck GE, Li S, Dobkin C, Brown WT.
    Am J Med Genet; 1994 Jul 15; 51(4):417-22. PubMed ID: 7943010
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  • 14. Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic.
    Pekarík V, Blazková M, Kozák L.
    Am J Med Genet; 1999 May 28; 84(3):214-6. PubMed ID: 10331594
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  • 16. Genetic diversity of the fragile X syndrome gene (FMR1) in a large Sub-Saharan West African population.
    Peprah EK, Allen EG, Williams SM, Woodard LM, Sherman SL.
    Ann Hum Genet; 2010 Jul 28; 74(4):316-25. PubMed ID: 20597902
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  • 17. Haplotype Analysis of DXS548 and FRAXAC1 Microsatellite Loci in Iranian Patients with Fragile X Syndrome.
    Aleyasin SA, Salamat F, Mirakhori M.
    Iran J Child Neurol; 2018 Jul 28; 12(1):36-46. PubMed ID: 29379561
    [Abstract] [Full Text] [Related]

  • 18. The identification of a (CGG)6AGG insertion within the CGG repeat of the FMR1 gene in Asians.
    Chen SH, Schoof JM, Buroker NE, Scott CR.
    Hum Genet; 1997 Jun 28; 99(6):793-5. PubMed ID: 9187675
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