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Journal Abstract Search

86 related items for PubMed ID: 1708201

  • 1. Physical and genetic mapping of the CDR gene with particular reference to its position with respect to the FRAXA site.
    Siniscalco M, Oberlé I, Melis P, Alhadeff B, Murray J, Filippi G, Mattioni T, Chen YT, Furneaux H, Old LJ.
    Am J Med Genet; 1991; 38(2-3):357-62. PubMed ID: 1708201
    [Abstract] [Full Text] [Related]

  • 2. 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; 79(3):219-27. PubMed ID: 3402993
    [Abstract] [Full Text] [Related]

  • 3. 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 Jul; 38(2-3):349-53. PubMed ID: 1673310
    [Abstract] [Full Text] [Related]

  • 4. 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. Mapping of a new RFLP marker RN1 (DXS369) close to the fragile site FRAXA on Xq27-q28.
    Oostra BA, Majoor-Krakauer DF, van Hemel JO, Bakker E, Callen DF, Schmidt M, van Oost BA.
    Am J Med Genet; 1991 Jan; 38(2-3):332-5. PubMed ID: 1673306
    [Abstract] [Full Text] [Related]

  • 8. Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site.
    Hirst MC, Bell MV, MacKinnon RN, Watson JE, Callen D, Sutherland G, Dahl N, Patterson MN, Schwartz C, Ledbetter D.
    Am J Med Genet; 1991 Jan; 38(2-3):354-6. PubMed ID: 1673311
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  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. 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; 45(2):304-9. PubMed ID: 2569270
    [Abstract] [Full Text] [Related]

  • 11. Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers.
    Glass IA, Pirrit LA, White EM, Bell MV, Davies KE, Cockburn F, Connor JM.
    Am J Med Genet; 1991 Aug; 38(2-3):298-304. PubMed ID: 1673301
    [Abstract] [Full Text] [Related]

  • 12. Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.
    Connor JM, Pirrit LA, Yates JR, Crossley JA, Imrie SJ, Colgan JM.
    J Med Genet; 1987 Jan; 24(1):14-22. PubMed ID: 2879932
    [Abstract] [Full Text] [Related]

  • 13. Carrier detection of the fragile X syndrome with flanking RFLP markers and linkage analysis.
    Väisänen ML, Kähkönen M, Leisti J.
    Am J Med Genet; 1987 Jan; 43(1-2):307-11. PubMed ID: 1351364
    [Abstract] [Full Text] [Related]

  • 14. DNA linkage analysis of 26 families with fragile X syndrome.
    Carpenter NJ.
    Am J Med Genet; 1991 Jan; 38(2-3):311-8. PubMed ID: 1673303
    [Abstract] [Full Text] [Related]

  • 15. 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 Jan; 38(2-3):328-31. PubMed ID: 2018075
    [Abstract] [Full Text] [Related]

  • 16. Carrier detection of the fragile X syndrome using flanking loci DXS98, DXS105, and DXS304.
    Dahl N, Malmgren H, Pettersson U, Holmgren G, Seemanová E, Gustavson KH.
    Am J Med Genet; 1991 Jan; 38(2-3):319-21. PubMed ID: 1673304
    [Abstract] [Full Text] [Related]

  • 17. 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
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.
    Brown WT, Ye W, Gross AC, Chan CB, Dobkin CS, Jenkins EC.
    Am J Med Genet; 1988 Jan; 30(1-2):551-66. PubMed ID: 2902796
    [Abstract] [Full Text] [Related]

  • 20. Physical mapping of probes proximal to the fragile X locus (FRAX) confirms the order F9-DXS105 (cX55.7)-DXS98 (4D8)-FRAXA.
    Sauer SM, Phelan MC, Richer CL, Schwartz CE.
    Cytogenet Cell Genet; 1989 Jan; 50(2-3):172-3. PubMed ID: 2776486
    [Abstract] [Full Text] [Related]

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