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Journal Abstract Search

143 related items for PubMed ID: 1670748

  • 1. Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA).
    Rousseau F, Vincent A, Rivella S, Heitz D, Triboli C, Maestrini E, Warren ST, Suthers GK, Goodfellow P, Mandel JL.
    Am J Hum Genet; 1991 Jan; 48(1):108-16. PubMed ID: 1670748
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  • 2. Genetic mapping of new RFLPs at Xq27-q28.
    Suthers GK, Oberlé I, Nancarrow J, Mulley JC, Hyland VJ, Wilson PJ, McCure J, Morris CP, Hopwood JJ, Mandel JL.
    Genomics; 1991 Jan; 9(1):37-43. PubMed ID: 1672291
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  • 7. Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.
    Suthers GK, Hyland VJ, Callen DF, Oberle I, Rocchi M, Thomas NS, Morris CP, Schwartz CE, Schmidt M, Ropers HH.
    Am J Hum Genet; 1990 Aug; 47(2):187-95. PubMed ID: 2378346
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  • 8. Linkage and risk assessment in fragile X families using new DNA probes at Xq27.
    Carpenter NJ, Swartz-Boyd J, Prichard JK, Lam T.
    Am J Med Genet; 1990 Aug; 43(1-2):312-9. PubMed ID: 1351365
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  • 9. Linkage homogeneity near the fragile X locus in normal and fragile X families.
    Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN.
    Genomics; 1991 Jul; 10(3):576-82. PubMed ID: 1889808
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  • 10. New informative polymorphism at the DXS304 locus, a close distal marker for the fragile X locus.
    Rousseau F, Vincent A, Oberlé I, Mandel JL.
    Hum Genet; 1990 Feb; 84(3):263-6. PubMed ID: 1968034
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  • 11. New distal marker closely linked to the fragile X locus.
    Hulsebos TJ, Oostra BA, Broersen S, Smits A, van Oost BA, Westerveld A.
    Hum Genet; 1991 Jul; 87(3):369-72. PubMed ID: 1677926
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  • 12. New polymorphisms at the DXS98 locus and confirmation of its location proximal to FRAXA by in situ hybridization.
    Schnur RE, Ledbetter SA, Ledbetter DH, Merry DE, Nussbaum RL.
    Am J Hum Genet; 1989 Feb; 44(2):248-54. PubMed ID: 2563194
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  • 13. Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304.
    Goonewardena P, Brown WT, Gross AC, Ferrando C, Dobkin C, Romano V, Bosco P, Ceratto N, Pettersson U, Dahl N.
    Am J Med Genet; 1991 Feb; 38(2-3):322-7. PubMed ID: 1673305
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  • 14. Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.
    Arveiler B, Oberlé I, Vincent A, Hofker MH, Pearson PL, Mandel JL.
    Am J Hum Genet; 1988 Feb; 42(2):380-9. PubMed ID: 2893549
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  • 15. A new DNA marker tightly linked to the fragile X locus (FRAXA).
    Suthers GK, Callen DF, Hyland VJ, Kozman HM, Baker E, Eyre H, Harper PS, Roberts SH, Hors-Cayla MC, Davies KE.
    Science; 1989 Dec 08; 246(4935):1298-300. PubMed ID: 2573953
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  • 16. Linkage relationships between DXS105, DXS98, and other polymorphic DNA markers flanking the fragile X locus.
    Carpenter NJ, Thibodeau SN, Brown WT.
    Am J Med Genet; 1991 Dec 08; 38(2-3):349-53. PubMed ID: 1673310
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  • 18. Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304).
    Dahl N, Goonewardena P, Malmgren H, Gustavson KH, Holmgren G, Seemanova E, Annerén G, Flood A, Pettersson U.
    Am J Hum Genet; 1989 Aug 08; 45(2):304-9. PubMed ID: 2569270
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  • 19. Multipoint linkage analysis of DXS369 and DXS304 in fragile X families.
    van Oost BA, Smits A, Dreesen JC, Smeets D, Perdon L, van Bennekom CA, Dahl N, Bakker E, Oostra BA.
    Am J Med Genet; 1991 Aug 08; 38(2-3):328-31. PubMed ID: 2018075
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  • 20. Linkage analysis using multiple DNA polymorphic markers in normal families and in families with fragile X syndrome.
    Thibodeau SN, Dorkins HR, Faulk KR, Berry R, Smith AC, Hagerman R, King A, Davies KE.
    Hum Genet; 1988 Jul 08; 79(3):219-27. PubMed ID: 3402993
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