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179 related items for PubMed ID: 1351033

  • 1. Linkage disequilibrium detected between myotonic dystrophy and the anonymous marker D19S63 in the Spanish population.
    Cobo A, Grinberg D, Balcells S, Vilageliu L, Gonzàlez-Duarte R, Baiget M.
    Hum Genet; 1992 May; 89(3):287-91. PubMed ID: 1351033
    [Abstract] [Full Text] [Related]

  • 2. Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.
    Nokelainen P, Alanen-Kurki L, Winqvist R, Falck B, Somer H, Leisti J, Johnson K, Savontaus ML, Peltonen L.
    Hum Genet; 1990 Oct; 85(5):541-5. PubMed ID: 1977684
    [Abstract] [Full Text] [Related]

  • 3. Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.
    MacKenzie AE, MacLeod HL, Hunter AG, Korneluk RG.
    Am J Hum Genet; 1989 Jan; 44(1):140-7. PubMed ID: 2562820
    [Abstract] [Full Text] [Related]

  • 4. DNA polymorphism and linkage disequilibrium within the apolipoprotein CII locus on human chromosome 19.
    MacKenzie AE, MacLeod HL, Leblond SC, Monteith N, Lahey D, Korneluk RG.
    Hum Hered; 1991 Jan; 41(3):188-94. PubMed ID: 1682238
    [Abstract] [Full Text] [Related]

  • 5. 3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations.
    Gennarelli M, Novelli G, Cobo A, Baiget M, Dallapiccola B.
    Hum Genet; 1991 Oct; 87(6):654-6. PubMed ID: 1682233
    [Abstract] [Full Text] [Related]

  • 6. Detection of linkage disequilibrium between the myotonic dystrophy locus and a new polymorphic DNA marker.
    Harley HG, Brook JD, Floyd J, Rundle SA, Crow S, Walsh KV, Thibault MC, Harper PS, Shaw DJ.
    Am J Hum Genet; 1991 Jul; 49(1):68-75. PubMed ID: 2063878
    [Abstract] [Full Text] [Related]

  • 7. The DM mutation; diagnostic applications in the Finnish population.
    Nokelainen P, Shelbourne P, Shaw D, Brook JD, Harley HG, Johnson K, Somer H, Savontaus ML, Peltonen L.
    Clin Genet; 1993 Apr; 43(4):190-5. PubMed ID: 8101149
    [Abstract] [Full Text] [Related]

  • 8. Identification of new DNA markers close to the myotonic dystrophy locus.
    Brook JD, Harley HG, Walsh KV, Rundle SA, Siciliano MJ, Harper PS, Shaw DJ.
    J Med Genet; 1991 Feb; 28(2):84-8. PubMed ID: 1672160
    [Abstract] [Full Text] [Related]

  • 9. Characteristics of myotonic dystrophy in Istria: molecular genetic approach. Part II: Analysis of genetic polymorphisms.
    Medica I, Logar N, Peterlin B.
    Coll Antropol; 2000 Dec; 24(2):287-94. PubMed ID: 11216395
    [Abstract] [Full Text] [Related]

  • 10. French myotonic dystrophy families show expansion of a CTG repeat in complete linkage disequilibrium with an intragenic 1 kb insertion.
    Lavedan C, Hofmann-Radvanyi H, Boileau C, Bonaïti-Pellié C, Savoy D, Shelbourne P, Duros C, Rabes JP, Dehaupas I, Luce S.
    J Med Genet; 1994 Jan; 31(1):33-6. PubMed ID: 8151634
    [Abstract] [Full Text] [Related]

  • 11. A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.
    Johnson K, Shelbourne P, Davies J, Buxton J, Nimmo E, Siciliano MJ, Bachinski LL, Anvret M, Harley H, Rundle S.
    Am J Hum Genet; 1990 Jun; 46(6):1073-81. PubMed ID: 1971149
    [Abstract] [Full Text] [Related]

  • 12. [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; 6(9):317-21. PubMed ID: 1687310
    [Abstract] [Full Text] [Related]

  • 13. Recombination events that locate myotonic dystrophy distal to APOC2 on 19q.
    Johnson K, Shelbourne P, Davies J, Buxton J, Nimmo E, Anvret M, Bonduelle M, Williamson B, Savontaus ML.
    Genomics; 1989 Nov; 5(4):746-51. PubMed ID: 2591962
    [Abstract] [Full Text] [Related]

  • 14. Founder effect and prevalence of myotonic dystrophy in South Africans: molecular studies.
    Goldman A, Krause A, Ramsay M, Jenkins T.
    Am J Hum Genet; 1996 Aug; 59(2):445-52. PubMed ID: 8755933
    [Abstract] [Full Text] [Related]

  • 15. 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; 28(2):89-91. PubMed ID: 2002492
    [Abstract] [Full Text] [Related]

  • 16. Haplotype analysis and LD detection at DM1 locus.
    Kumar A, Agarwal S, Pradhan S.
    Gene; 2015 Aug 01; 567(1):45-50. PubMed ID: 25934189
    [Abstract] [Full Text] [Related]

  • 17. Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).
    Brunner HG, Korneluk RG, Coerwinkel-Driessen M, MacKenzie A, Smeets H, Lambermon HM, van Oost BA, Wieringa B, Ropers HH.
    Hum Genet; 1989 Mar 01; 81(4):308-10. PubMed ID: 2703233
    [Abstract] [Full Text] [Related]

  • 18. Myotonic dystrophy: molecular analysis of Israeli patients.
    Abeliovich D, Lerer I, Pashut-Lavon I, Cohen T.
    Biomed Pharmacother; 1994 Mar 01; 48(8-9):373-80. PubMed ID: 7858174
    [Abstract] [Full Text] [Related]

  • 19. Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19.
    Yamaoka LH, Pericak-Vance MA, Speer MC, Gaskell PC, Stajich J, Haynes C, Hung WY, Laberge C, Thibault MC, Mathieu J.
    Neurology; 1990 Feb 01; 40(2):222-6. PubMed ID: 2300239
    [Abstract] [Full Text] [Related]

  • 20. Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy.
    Walsh KV, Harley HG, Brook JD, Rundle SA, Sarfarazi M, Harper PS, Shaw DJ.
    Hum Genet; 1990 Aug 01; 85(3):305-10. PubMed ID: 1975560
    [Abstract] [Full Text] [Related]

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