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Journal Abstract Search

126 related items for PubMed ID: 1673305

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  • 4. 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; 38(2-3):349-53. PubMed ID: 1673310
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  • 5. 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; 38(2-3):319-21. PubMed ID: 1673304
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  • 6. 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; 38(2-3):298-304. PubMed ID: 1673301
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  • 7. DNA linkage analysis of 26 families with fragile X syndrome.
    Carpenter NJ.
    Am J Med Genet; 1991; 38(2-3):311-8. PubMed ID: 1673303
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  • 8. 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
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  • 10. New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA interval.
    Oberlé I, Vincent A, Abbadi N, Rousseau F, Hupkes PE, Hors-Cayla MC, Gilgenkrantz S, Oostra BA, Mandel JL.
    Am J Med Genet; 1991 Jul; 38(2-3):336-42. PubMed ID: 1673307
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  • 14. The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.
    Vincent A, Dahl N, Oberlé I, Hanauer A, Mandel JL, Malmgren H, Pettersson U.
    Genomics; 1989 Nov; 5(4):797-801. PubMed ID: 2574147
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  • 15. 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
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  • 16. Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8.
    Brown WT, Gross AC, Goonewardena P, Ferrando C, Dobkin C, Jenkins EC.
    Am J Med Genet; 1991 Jan; 38(2-3):343-6. PubMed ID: 1673308
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  • 20. Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).
    Mulley J, Turner G, Bain S, Sutherland GR.
    Am J Med Genet; 1988 Jan; 30(1-2):567-80. PubMed ID: 2902797
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