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Journal Abstract Search

58 related items for PubMed ID: 1350853

  • 1. 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]

  • 2. [Presymptomatic DNA diagnosis in Huntington chorea with linked DNA markers].
    Thies U, Schröder K, Bockel B, Zoll B, Lange H.
    Nervenarzt; 1991 Oct 02; 62(10):615-20. PubMed ID: 1684226
    [No Abstract] [Full Text] [Related]

  • 3. DNA-based prenatal diagnosis of heritable skin diseases.
    Christiano AM, Uitto J.
    Arch Dermatol; 1993 Nov 02; 129(11):1455-9. PubMed ID: 7902070
    [Abstract] [Full Text] [Related]

  • 4. [Gene diagnosis for hepatolenticular degeneration by genetic linkage analysis with four short tandem repeat polymorphisms].
    Wu Z, Yu L, Wang N.
    Zhonghua Yi Xue Za Zhi; 1996 Aug 02; 76(8):578-81. PubMed ID: 9275468
    [Abstract] [Full Text] [Related]

  • 5. Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis.
    Figus A, Lampis R, Devoto M, Ristaldi MS, Ideo A, de Virgilis S, Nurchi AM, Corrias A, Corda R, Lai ME.
    J Med Genet; 1989 Feb 02; 26(2):78-82. PubMed ID: 2563776
    [Abstract] [Full Text] [Related]

  • 6. Prenatal exclusion of choroideremia.
    van den Hurk JA, van Zandvoort PM, Brunsmann F, Pawlowitzki IH, Holzgreve W, Szabo P, Cremers FP, van Oost BA.
    Am J Med Genet; 1992 Dec 01; 44(6):822-3. PubMed ID: 1362326
    [Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French family.
    Lucotte G, Berriche S, David F, Mariotti M, Turpin JC.
    Genet Couns; 1994 Dec 01; 5(2):171-4. PubMed ID: 7917127
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of cystic fibrosis by chorionic villus sampling using 12 polymorphic deoxyribonucleic acid markers.
    Nugent CE, Gravius T, Green P, Larsen JW, MacMillin MD, Donis-Keller H.
    Obstet Gynecol; 1988 Feb 01; 71(2):213-5. PubMed ID: 3422111
    [Abstract] [Full Text] [Related]

  • 9. [Clinical application of chromosome haplotype analysis and mutation analysis to the diagnosis of Wilson's disease].
    Shi X, Ling Q, Xia J, Wu H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1999 Feb 10; 16(1):32-5. PubMed ID: 9950703
    [Abstract] [Full Text] [Related]

  • 10. Reproductive decisions after prenatal diagnosis in neurofibromatosis type 1: importance of genetic counseling.
    Terzi YK, Oguzkan-Balci S, Anlar B, Aysun S, Guran S, Ayter S.
    Genet Couns; 2009 Feb 10; 20(2):195-202. PubMed ID: 19650418
    [Abstract] [Full Text] [Related]

  • 11. 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 Feb 10; 5(2):183-5. PubMed ID: 7917130
    [Abstract] [Full Text] [Related]

  • 12. Carrier detection and prenatal diagnosis in haemophilia A and B.
    Chistolini A, Papacchini M, Mazzucconi MG, La Verde G, Arcieri R, Ferrari A, Paesano R, Pachi A, Mariani G.
    Haematologica; 1990 Feb 10; 75(5):424-8. PubMed ID: 1982946
    [Abstract] [Full Text] [Related]

  • 13. Predictive testing for Wilson's disease using tightly linked and flanking DNA markers.
    Farrer LA, Bowcock AM, Hebert JM, Bonné-Tamir B, Sternlieb I, Giagheddu M, St George-Hyslop P, Frydman M, Lössner J, Demelia L.
    Neurology; 1991 Jul 10; 41(7):992-9. PubMed ID: 2067662
    [Abstract] [Full Text] [Related]

  • 14. Prenatal exclusion testing for Huntington disease using the polymerase chain reaction.
    McIntosh I, Curtis A, Millan FA, Brock DJ.
    Am J Med Genet; 1989 Feb 10; 32(2):274-6. PubMed ID: 2564738
    [Abstract] [Full Text] [Related]

  • 15. The usefulness of three biallelic restriction fragment length polymorphisms versus a polymorphic dinucleotide tandem repeat polymorphism at the low-density-lipoprotein receptor gene locus for diagnosis of familial hypercholesterolemia.
    Weiss N, Gudnasson V, Ostwald P, Humphries S, Schuster H, Keller C.
    Dis Markers; 1997 Nov 10; 13(3):141-51. PubMed ID: 9405927
    [Abstract] [Full Text] [Related]

  • 16. Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes.
    Haines JL, Ozelius L, St George-Hyslop P, Wexler NS, Gusella JF, Conneally PM.
    Genet Epidemiol; 1988 Nov 10; 5(6):375-80. PubMed ID: 2905314
    [Abstract] [Full Text] [Related]

  • 17. The clinical applications of DNA polymorphisms.
    Thein SL, Wainscoat JS.
    Dis Markers; 1986 Oct 10; 4(3):203-18. PubMed ID: 2898316
    [No Abstract] [Full Text] [Related]

  • 18. Molecular genetic strategies to investigate Huntington's disease.
    Gilliam TC, Gusella JF, Lehrach H.
    Adv Neurol; 1988 Oct 10; 48():17-29. PubMed ID: 2891255
    [No Abstract] [Full Text] [Related]

  • 19. A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group.
    Science; 1992 Oct 02; 258(5079):148-62. PubMed ID: 1359639
    [No Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis of cystic fibrosis by using linked DNA markers in 138 pregnancies at 1-in-4 risk.
    Feldman GL, Lewiston N, Fernbach SD, O'Brien WE, Williamson R, Wainwright BJ, Beaudet AL.
    Am J Med Genet; 1989 Jun 02; 33(2):238-41. PubMed ID: 2569827
    [Abstract] [Full Text] [Related]

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