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Journal Abstract Search

167 related items for PubMed ID: 2575669

  • 1. Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markers.
    Norman AM, Floyd JL, Meredith AL, Harper PS.
    J Med Genet; 1989 Dec; 26(12):750-4. PubMed ID: 2575669
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  • 3. Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.
    Meredith AL, Huson SM, Lunt PW, Sarfarazi M, Harley HG, Brook JD, Shaw DJ, Harper PS.
    Br Med J (Clin Res Ed); 1986 Nov 22; 293(6558):1353-6. PubMed ID: 2878705
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  • 4. Prenatal diagnosis of myotonic dystrophy using closely linked flanking markers.
    Lavedan C, Hofmann H, Shelbourne P, Duros C, Savoy D, Johnson K, Junien C.
    J Med Genet; 1991 Feb 22; 28(2):89-91. PubMed ID: 2002492
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  • 5. Five years experience of predictive testing for myotonic dystrophy using linked DNA markers.
    Reardon W, Floyd JL, Myring J, Lazarou LP, Meredith AL, Harper PS.
    Am J Med Genet; 1992 Aug 01; 43(6):1006-11. PubMed ID: 1415325
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  • 6. The apolipoprotein CII gene: subchromosomal localisation and linkage to the myotonic dystrophy locus.
    Shaw DJ, Meredith AL, Sarfarazi M, Huson SM, Brook JD, Myklebost O, Harper PS.
    Hum Genet; 1985 Aug 01; 70(3):271-3. PubMed ID: 2991117
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  • 13. 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 Aug 01; 5 ( Pt 1)():93-8. PubMed ID: 1676377
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  • 17. [Myotonic dystrophy of Steinert].
    Junien C.
    J Genet Hum; 1989 Jan 01; 37(1):51-4. PubMed ID: 2565953
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  • 18. Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.
    Shaw DJ, Meredith AL, Sarfarazi M, Harley HG, Huson SM, Brook JD, Bufton L, Litt M, Mohandas T, Harper PS.
    Hum Genet; 1986 Nov 01; 74(3):262-6. PubMed ID: 2877933
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  • 19. Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): application to myotonic dystrophy diagnosis.
    Lavedan C, Duros C, Savoy D, Leblond S, Bailly J, Korneluk R, Junien C.
    Genomics; 1990 Dec 01; 8(4):739-40. PubMed ID: 1980487
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  • 20. [Application of the polymerase chain reaction technique (PCR) to the molecular diagnosis of myotonic dystrophy].
    Cobo AM, Martínez JM, López de Munain A, Baiget M.
    Neurologia; 1991 Nov 01; 6(9):317-21. PubMed ID: 1687310
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