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Journal Abstract Search

150 related items for PubMed ID: 2888310

  • 1. A new DNA probe proximal to and closely linked to fragile X.
    Carpenter NJ, Veenema H, Bakker E, Hofker MH, Pearson PL.
    Am J Med Genet; 1987 Jul; 27(3):731-2. PubMed ID: 2888310
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  • 2. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.
    Mulley JC, Gedeon AK, Thorn KA, Bates LJ, Sutherland GR.
    Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048
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  • 3. From hemophilia B to hemophilia A via the fragile X locus: genes and recombination in the distal region of the human X chromosome long arm.
    Oberlé I, Mandel JL.
    Horiz Biochem Biophys; 1986 Jun; 8():51-89. PubMed ID: 2875934
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  • 4. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P, Dahl N, Gustavson KH, Holmgren G, Pettersson U.
    Ups J Med Sci Suppl; 1987 Jun; 44():155-64. PubMed ID: 2895524
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  • 5. [Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics].
    Benítez J, Fernández E, Ramos C, Nunes V, del Río E, Baiget M.
    Rev Clin Esp; 1989 Apr; 184(7):364-6. PubMed ID: 2570446
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  • 10. The fragile-X syndrome, IV. Progress towards the identification of linked restriction fragment length variants (RFLVs).
    Holden JJ, Wang HS, White BN.
    Am J Med Genet; 1984 Jan; 17(1):259-73. PubMed ID: 6324593
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  • 12. RN1, a new polymorphic marker near the fragile X locus. (HGM10 assignment DXS 369).
    Hupkes PE, van Bennekom CA, van Oost BA, Oostra BA.
    Nucleic Acids Res; 1990 Feb 11; 18(3):692. PubMed ID: 1968631
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  • 14. 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 11; 44(2):248-54. PubMed ID: 2563194
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  • 16. A new RFLP with StuI and probe cX55.7 (DXS105) and its usefulness in carrier analysis of fragile X syndrome.
    Rekilä AM, Väisänen ML, Kähkönen M, Leisti J, Winqvist R.
    Hum Genet; 1988 Oct 11; 80(2):193. PubMed ID: 2902001
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  • 17. 46,XY/47,XYY male with the fragile X syndrome: cytogenetic and molecular studies.
    Milunsky A, Huang X, Amos JA, Herskowitz J, Farrer LA, Wyandt HE.
    Am J Med Genet; 1993 Mar 01; 45(5):589-93. PubMed ID: 8096117
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  • 18. 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 01; 5(4):797-801. PubMed ID: 2574147
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  • 19. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
    Voelckel MA, Philip N, Piquet C, Pellissier MC, Oberlé I, Birg F, Mattei MG, Mattei JF.
    Hum Genet; 1989 Mar 01; 81(4):353-7. PubMed ID: 2564838
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