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PUBMED FOR HANDHELDS

Journal Abstract Search

190 related items for PubMed ID: 1684226

  • 41. Prenatal testing for Huntington disease.
    Corson V, Quaid K, Kasch L, Kazazian HH.
    Birth Defects Orig Artic Ser; 1990; 26(3):226-30. PubMed ID: 2151181
    [No Abstract] [Full Text] [Related]

  • 42. [Presymptomatic diagnosis in Huntington chorea families using the gene amplification technique].
    Lucotte G, Berriche S, Petit MC, Burckel A, Turpin JC.
    Rev Neurol (Paris); 1991; 147(8-9):602-4. PubMed ID: 1835796
    [Abstract] [Full Text] [Related]

  • 43. Identification of carriers by screening for delta F508 deletion in a multi-generation cystic fibrosis family.
    Claustres M, Desgeorges M, Kjellberg P, Demaille J.
    Genet Couns; 1990; 1(3-4):211-7. PubMed ID: 1982988
    [Abstract] [Full Text] [Related]

  • 44. Psychiatric morbidity associated with early clinical diagnosis of Huntington disease in a predictive testing program.
    Lam RW, Bloch M, Jones BD, Marcus AM, Fox S, Amman W, Hayden MR.
    J Clin Psychiatry; 1988 Nov; 49(11):444-7. PubMed ID: 2972696
    [Abstract] [Full Text] [Related]

  • 45. At risk for Huntington's disease: who should know what and when?
    Rosenfeld A.
    Hastings Cent Rep; 1984 Jun; 14(3):5-8. PubMed ID: 6086548
    [Abstract] [Full Text] [Related]

  • 46. Response to Hayden, Bloch, Fox and Crauford: presymptomatic and prenatal testing in Huntington disease.
    Shaw MW.
    Am J Med Genet; 1987 Nov; 28(3):765-6. PubMed ID: 2962496
    [No Abstract] [Full Text] [Related]

  • 47. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
    Mulley JC, Gedeon AK, Haan EA, Sheffield LJ, White SJ, Bates LJ, Robertson EF, Sutherland GR.
    Aust Paediatr J; 1988 Nov; 24 Suppl 1():92-7. PubMed ID: 3202740
    [Abstract] [Full Text] [Related]

  • 48. Pitfalls in counseling for predictive testing in Huntington disease.
    Demyttenaere K, Evers-Kiebooms G, Decruyenaere M.
    Birth Defects Orig Artic Ser; 1992 Nov; 28(1):105-11. PubMed ID: 1340218
    [No Abstract] [Full Text] [Related]

  • 49. First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDR.
    Herrmann FH, Kruse T, Wehnert M, Vogel G, Wulff K.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1988 Nov; 115(4):489-93. PubMed ID: 2465959
    [Abstract] [Full Text] [Related]

  • 50. Characterization of new probes for diagnosis of polycystic kidney disease (PKD1).
    Breuning MH, Verwest A, Ijdo J, Saris JJ, Keith T, Reeders ST, van Ommen GJ, Pearson PL.
    Prog Clin Biol Res; 1989 Nov; 305():69-75. PubMed ID: 2569743
    [No Abstract] [Full Text] [Related]

  • 51. [Psychotic syndrome in chorea Huntington].
    Känzig S, Eichorn M.
    Psychiatr Prax; 2003 Jul; 30(5):286-7. PubMed ID: 12947934
    [No Abstract] [Full Text] [Related]

  • 52. Predictive testing for Huntington disease and the right not to know. Some ethical reflections.
    de Wert G.
    Birth Defects Orig Artic Ser; 1992 Jul; 28(1):133-8. PubMed ID: 1340223
    [No Abstract] [Full Text] [Related]

  • 53. [Genetic counseling in prenatal diagnosis of cystic fibrosis].
    Wolff G, Mayerová A.
    Monatsschr Kinderheilkd; 1991 May; 139(5):275-81. PubMed ID: 1870597
    [Abstract] [Full Text] [Related]

  • 54. Mosaicism in clinical practice exemplified by prenatal diagnosis in retinoblastoma.
    Castéra L, Gauthier-Villars M, Dehainault C, Michaux D, Benachi A, Lumbroso-Le Rouic L, Stoppa-Lyonnet D, Houdayer C.
    Prenat Diagn; 2011 Nov; 31(11):1106-8. PubMed ID: 21905051
    [No Abstract] [Full Text] [Related]

  • 55. Presymptomatic testing for Huntington's disease.
    Bird SJ.
    JAMA; 1985 Jun 14; 253(22):3286-91. PubMed ID: 3158756
    [Abstract] [Full Text] [Related]

  • 56. 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 14; 26(2):83-5. PubMed ID: 2563777
    [Abstract] [Full Text] [Related]

  • 57. Huntington's disease: recent progress in gene mapping and potential local application in Singapore.
    Wong MC, Ng IS.
    Ann Acad Med Singap; 1993 May 14; 22(3 Suppl):534-6. PubMed ID: 8105747
    [Abstract] [Full Text] [Related]

  • 58. The prenatal exclusion test for Huntington's disease: experience in the west of Scotland, 1986-1993.
    Tolmie JL, Davidson HR, May HM, McIntosh K, Paterson JS, Smith B.
    J Med Genet; 1995 Feb 14; 32(2):97-101. PubMed ID: 7760329
    [Abstract] [Full Text] [Related]

  • 59. Attitudes of persons at risk and their partners toward predictive testing.
    Jacopini GA, D'Amico R, Frontali M, Vivona G.
    Birth Defects Orig Artic Ser; 1992 Feb 14; 28(1):113-7. PubMed ID: 1340220
    [No Abstract] [Full Text] [Related]

  • 60. Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington's disease.
    Brandt J, Quaid KA, Folstein SE, Garber P, Maestri NE, Abbott MH, Slavney PR, Franz ML, Kasch L, Kazazian HH.
    JAMA; 1989 Jun 02; 261(21):3108-14. PubMed ID: 2523979
    [Abstract] [Full Text] [Related]

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