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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

190 related items for PubMed ID: 1684226

  • 21. Huntington disease: estimation of heterozygote status using linked genetic markers.
    Conneally PM, Wallace MR, Gusella JF, Wexler NS.
    Genet Epidemiol; 1984; 1(1):81-8. PubMed ID: 6242401
    [Abstract] [Full Text] [Related]

  • 22. Decision making in Huntington's disease and cystic fibrosis.
    Evers-Kiebooms G.
    Birth Defects Orig Artic Ser; 1987; 23(2):115-49. PubMed ID: 2885041
    [No Abstract] [Full Text] [Related]

  • 23. [DNA markers linked to Huntington's disease (D4S10 and D4S95) in Spanish families: preliminary results].
    Benítez J, Ramos C, Fernández E, Ayuso C, Yébenes J.
    Rev Clin Esp; 1992 Apr; 190(6):299-301. PubMed ID: 1350862
    [Abstract] [Full Text] [Related]

  • 24. A new DNA probe of potential use for diagnosis of the fragile-X syndrome.
    Lucotte G.
    Ann Genet; 1990 Apr; 33(2):109-10. PubMed ID: 1978629
    [Abstract] [Full Text] [Related]

  • 25. [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
    [Abstract] [Full Text] [Related]

  • 26. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.
    Tuffery S, Moine P, Sarda P, Lefort G, Boulot P, Demaille J, Claustres M.
    Genet Couns; 1994 Apr; 5(2):183-5. PubMed ID: 7917130
    [Abstract] [Full Text] [Related]

  • 27.
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  • 28. [Huntington chorea: perspective changes in presymptomatic diagnosis (updating synthetic review)].
    Borri G.
    Riv Neurol; 1989 Apr; 59(6):223-8. PubMed ID: 2534779
    [Abstract] [Full Text] [Related]

  • 29. [Prenatal diagnosis of hereditary hemoglobinopathies].
    Cao A, Pirastu M, Rosatelli C.
    Haematologica; 1989 Oct; 74(5 Suppl):213-22. PubMed ID: 2574134
    [No Abstract] [Full Text] [Related]

  • 30. Prenatal diagnosis of Wilson's disease by analysis of DNA polymorphism.
    Cossu P, Pirastu M, Nucaro A, Figus A, Balestrieri A, Borrone C, Giacchino R, Devoto M, Monni G, Cao A.
    N Engl J Med; 1992 Jul 02; 327(1):57. PubMed ID: 1350853
    [No Abstract] [Full Text] [Related]

  • 31. DNA analysis of haemophilia A families from southern France. Experience of a hospital laboratory.
    Aguilar-Martinez P, Fabre N, Navarro R, Schved JF, Gris JC, Romey MC, Demaille J, Claustres M.
    Genet Couns; 1993 Jul 02; 4(4):311-9. PubMed ID: 7906519
    [Abstract] [Full Text] [Related]

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  • 33. 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]

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  • 36. Genetic jeopardy and the new clairvoyance.
    Wexler NS.
    Prog Med Genet; 1985 Jun 06; 6():277-304. PubMed ID: 2941821
    [No Abstract] [Full Text] [Related]

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  • 38. Genetic counselling for myotonic dystrophy: a comparison of lens examination and DNA linkage studies.
    Longstaff S, Curtis D, Quick J, Talbot J.
    Eye (Lond); 1991 Jun 06; 5 ( Pt 1)():93-8. PubMed ID: 1676377
    [Abstract] [Full Text] [Related]

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