These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

120 related items for PubMed ID: 2900522

  • 1. Huntington's disease: prediction and prevention.
    Harper PS, Quarrell OW, Youngman S.
    Philos Trans R Soc Lond B Biol Sci; 1988 Jun 15; 319(1194):285-98. PubMed ID: 2900522
    [Abstract] [Full Text] [Related]

  • 2. Prenatal and adult presymptomatic testing for Huntington's disease.
    Turner DR, Haan EA, Jacka E, Kalucy RS, Burns RJ, Willoughby JO, Crabb R.
    Med J Aust; 1988 Jun 06; 148(11):567, 570-3. PubMed ID: 2897620
    [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 06; 81(2):188-90. PubMed ID: 2563253
    [Abstract] [Full Text] [Related]

  • 4. Genetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure?
    Misra VP, Baraitser M, Harding AE.
    Mov Disord; 1988 Jan 06; 3(3):233-6. PubMed ID: 2973561
    [Abstract] [Full Text] [Related]

  • 5. Genetic prediction and family structure in Huntington's chorea.
    Harper PS, Sarfarazi M.
    Br Med J (Clin Res Ed); 1985 Jun 29; 290(6486):1929-31. PubMed ID: 3159461
    [Abstract] [Full Text] [Related]

  • 6. 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 29; 43(3):150-6. PubMed ID: 8098998
    [Abstract] [Full Text] [Related]

  • 7. Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families.
    Harper PS, Youngman S, Anderson MA, Sarfarazi M, Quarrell O, Tanzi R, Shaw D, Wallace P, Conneally PM, Gusella JF.
    J Med Genet; 1985 Dec 29; 22(6):447-50. PubMed ID: 3001311
    [Abstract] [Full Text] [Related]

  • 8. 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 29; 25(9):577-88. PubMed ID: 2903248
    [Abstract] [Full Text] [Related]

  • 9. Predictive testing for Huntington's disease with use of a linked DNA marker.
    Meissen GJ, Myers RH, Mastromauro CA, Koroshetz WJ, Klinger KW, Farrer LA, Watkins PA, Gusella JF, Bird ED, Martin JB.
    N Engl J Med; 1988 Mar 03; 318(9):535-42. PubMed ID: 2893260
    [Abstract] [Full Text] [Related]

  • 10. Predictive testing for Huntington's disease: after the gene. The United Kingdom Huntington's Disease Prediction Consortium.
    Simpson SA, Harding AE.
    J Med Genet; 1993 Dec 03; 30(12):1036-8. PubMed ID: 8133503
    [Abstract] [Full Text] [Related]

  • 11. 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 03; 14(4-6):524-9. PubMed ID: 1363459
    [Abstract] [Full Text] [Related]

  • 12. [Genetic counseling on a molecular basis for Huntington's chorea].
    Cassiman JJ.
    J Genet Hum; 1989 Jan 03; 37(1):13-24. PubMed ID: 2565951
    [Abstract] [Full Text] [Related]

  • 13. [Use of polymorphous DNA probes in the study of French families with Huntington's chorea].
    Lucotte G, Berriche S, Burckel A, Turpin JC.
    Rev Neurol (Paris); 1990 Jan 03; 146(4):303-5. PubMed ID: 1972803
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Different options for prenatal testing for Huntington's disease using DNA probes.
    Fahy M, Robbins C, Bloch M, Turnell RW, Hayden MR.
    J Med Genet; 1989 Jun 26; 26(6):353-7. PubMed ID: 2525622
    [Abstract] [Full Text] [Related]

  • 16. Utilisation of predictive, prenatal and diagnostic testing for Huntington's disease in Johannesburg.
    Kromberg JG, Krause A, Spurdle AB, Temlett JA, Lucas M, Rodseth D, Stevens G, Jenkins T.
    S Afr Med J; 1999 Jul 26; 89(7):774-8. PubMed ID: 10470316
    [Abstract] [Full Text] [Related]

  • 17. Prenatal exclusion testing for Huntington's disease: a problem of too much information.
    Millan FA, Curtis A, Mennie M, Holloway S, Boxer M, Faed MJ, Crawford JW, Liston WA, Brock DJ.
    J Med Genet; 1989 Feb 26; 26(2):83-5. PubMed ID: 2563777
    [Abstract] [Full Text] [Related]

  • 18. A polymorphic DNA marker genetically linked to Huntington's disease.
    Gusella JF, Wexler NS, Conneally PM, Naylor SL, Anderson MA, Tanzi RE, Watkins PC, Ottina K, Wallace MR, Sakaguchi AY.
    Nature; 1989 Feb 26; 306(5940):234-8. PubMed ID: 6316146
    [Abstract] [Full Text] [Related]

  • 19. A DNA segment encoding two genes very tightly linked to Huntington's disease.
    Gilliam TC, Bucan M, MacDonald ME, Zimmer M, Haines JL, Cheng SV, Pohl TM, Meyers RH, Whaley WL, Allitto BA.
    Science; 1987 Nov 13; 238(4829):950-2. PubMed ID: 2890209
    [Abstract] [Full Text] [Related]

  • 20. Absence of close linkage between benign hereditary chorea and the locus D4S10 (probe G8).
    Quarrell OW, Youngman S, Sarfarazi M, Harper PS.
    J Med Genet; 1988 Mar 13; 25(3):191-4. PubMed ID: 2895189
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.