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Journal Abstract Search

159 related items for PubMed ID: 9382108

  • 1. Risk reversals in predictive testing for Huntington disease.
    Almqvist E, Adam S, Bloch M, Fuller A, Welch P, Eisenberg D, Whelan D, Macgregor D, Meschino W, Hayden MR.
    Am J Hum Genet; 1997 Oct; 61(4):945-52. PubMed ID: 9382108
    [Abstract] [Full Text] [Related]

  • 2. Attitudes toward direct predictive testing for the Huntington disease gene. Relevance for other adult-onset disorders. The Canadian Collaborative Group on Predictive Testing for Huntington Disease.
    Babul R, Adam S, Kremer B, Dufrasne S, Wiggins S, Huggins M, Theilmann J, Bloch M, Hayden MR.
    JAMA; 1993 Nov 17; 270(19):2321-5. PubMed ID: 8230594
    [Abstract] [Full Text] [Related]

  • 3. Presymptomatic testing for Huntington's disease. A case complicated by recombination within the D4S10 locus.
    Curtis A, Millan F, Holloway S, Mennie M, Crosbie A, Raeburn JA, Brock DJ.
    Hum Genet; 1989 Jan 17; 81(2):188-90. PubMed ID: 2563253
    [Abstract] [Full Text] [Related]

  • 4. Improved predictive testing for Huntington disease by using three linked DNA markers.
    Hayden MR, Robbins C, Allard D, Haines J, Fox S, Wasmuth J, Fahy M, Bloch M.
    Am J Hum Genet; 1988 Nov 17; 43(5):689-94. PubMed ID: 2973229
    [Abstract] [Full Text] [Related]

  • 5. Huntington's disease: predictive testing and the molecular genetics laboratory.
    Lazarou LP, Meredith AL, Myring JM, Tyler A, Morris M, Ball DM, Harper PS.
    Clin Genet; 1993 Mar 17; 43(3):150-6. PubMed ID: 8098998
    [Abstract] [Full Text] [Related]

  • 6. Proceed with care: direct predictive testing for Huntington disease.
    Benjamin CM, Adam S, Wiggins S, Theilmann JL, Copley TT, Bloch M, Squitieri F, McKellin W, Cox S, Brown SA.
    Am J Hum Genet; 1994 Oct 17; 55(4):606-17. PubMed ID: 7942838
    [Abstract] [Full Text] [Related]

  • 7. Linkage disequilibrium and modification of risk for Huntington disease.
    Adam S, Theilmann J, Buetow K, Hedrick A, Collins C, Weber B, Huggins M, Hayden M.
    Am J Hum Genet; 1991 Mar 17; 48(3):595-603. PubMed ID: 1671809
    [Abstract] [Full Text] [Related]

  • 8. Recombination of 4p16 DNA markers in an unusual family with Huntington disease.
    Pritchard C, Zhu N, Zuo J, Bull L, Pericak-Vance MA, Vance JM, Roses AD, Milatovich A, Francke U, Cox DR.
    Am J Hum Genet; 1992 Jun 17; 50(6):1218-30. PubMed ID: 1350884
    [Abstract] [Full Text] [Related]

  • 9. Predictive, pre-natal and diagnostic genetic testing for Huntington's disease: the experience in Canada from 1987 to 2000.
    Creighton S, Almqvist EW, MacGregor D, Fernandez B, Hogg H, Beis J, Welch JP, Riddell C, Lokkesmoe R, Khalifa M, MacKenzie J, Sajoo A, Farrell S, Robert F, Shugar A, Summers A, Meschino W, Allingham-Hawkins D, Chiu T, Hunter A, Allanson J, Hare H, Schween J, Collins L, Sanders S, Greenberg C, Cardwell S, Lemire E, MacLeod P, Hayden MR.
    Clin Genet; 2003 Jun 17; 63(6):462-75. PubMed ID: 12786753
    [Abstract] [Full Text] [Related]

  • 10. Considerations in using linkage analysis as a presymptomatic test for Huntington's disease.
    Farrer LA, Myers RH, Cupples LA, Conneally PM.
    J Med Genet; 1988 Sep 17; 25(9):577-88. PubMed ID: 2903248
    [Abstract] [Full Text] [Related]

  • 11. Ethical and legal dilemmas arising during predictive testing for adult-onset disease: the experience of Huntington disease.
    Huggins M, Bloch M, Kanani S, Quarrell OW, Theilman J, Hedrick A, Dickens B, Lynch A, Hayden M.
    Am J Hum Genet; 1990 Jul 17; 47(1):4-12. PubMed ID: 1971997
    [Abstract] [Full Text] [Related]

  • 12. Predictive testing for Huntington's disease with linked DNA markers.
    Brock DJ, Mennie M, Curtis A, Millan FA, Barron L, Raeburn JA, Dinwoodie D, Holloway S, Crosbie A, Wright A.
    Lancet; 1989 Aug 26; 2(8661):463-6. PubMed ID: 2570183
    [Abstract] [Full Text] [Related]

  • 13. Testing the test--why pursue a better test for Huntington disease?
    Timman R, Maat-Kievit A, Brouwer-DudokdeWit C, Zoeteweij M, Breuning MH, Tibben A.
    Am J Med Genet B Neuropsychiatr Genet; 2003 Feb 26; 117B(1):79-85. PubMed ID: 12555240
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  • 15. Singleton births after routine preimplantation genetic diagnosis using exclusion testing (D4S43 and D4S126) for Huntington's disease.
    Jasper MJ, Hu DG, Liebelt J, Sherrin D, Watson R, Tremellen KP, Hussey ND.
    Fertil Steril; 2006 Mar 26; 85(3):597-602. PubMed ID: 16500325
    [Abstract] [Full Text] [Related]

  • 16. Null alleles at the Huntington disease locus: implications for diagnostics and CAG repeat instability.
    Williams LC, Hegde MR, Nagappan R, Faull RL, Giles J, Winship I, Snow K, Love DR.
    Genet Test; 2000 Mar 26; 4(1):55-60. PubMed ID: 10794362
    [Abstract] [Full Text] [Related]

  • 17. Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region.
    Weber B, Hedrick A, Andrew S, Riess O, Collins C, Kowbel D, Hayden MR.
    Am J Hum Genet; 1992 Feb 26; 50(2):382-93. PubMed ID: 1346482
    [Abstract] [Full Text] [Related]

  • 18. Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90.
    Robbins C, Theilmann J, Youngman S, Haines J, Altherr MJ, Harper PS, Payne C, Junker A, Wasmuth J, Hayden MR.
    Am J Hum Genet; 1989 Mar 26; 44(3):422-5. PubMed ID: 2521771
    [Abstract] [Full Text] [Related]

  • 19. Perspectives towards predictive testing in Huntington disease.
    Nagaraja SM, Jain S, Muthane UB.
    Neurol India; 2006 Dec 26; 54(4):359-62. PubMed ID: 17114842
    [Abstract] [Full Text] [Related]

  • 20. Genetic linkage analysis and presymptomatic testing in Huntington's disease. First report in Italy.
    Di Maio L, Boiano S, Squitieri F, Napolitano G, Cocozza S, Campanella G, Battistuzzi G.
    Acta Neurol (Napoli); 1992 Dec 26; 14(4-6):524-9. PubMed ID: 1363459
    [Abstract] [Full Text] [Related]

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