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Journal Abstract Search

174 related items for PubMed ID: 1977684

  • 1. 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
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  • 2. 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
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  • 6. 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
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  • 7. 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
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  • 10. 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
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  • 11. 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 01; 49(1):68-75. PubMed ID: 2063878
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  • 12. 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
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  • 13. Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q.
    Harley HG, Walsh KV, Rundle S, Brook JD, Sarfarazi M, Koch MC, Floyd JL, Harper PS, Shaw DJ.
    Hum Genet; 1991 May 01; 87(1):73-80. PubMed ID: 2037285
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  • 14. 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
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  • 15. A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.
    Brunner HG, Smeets H, Lambermon HM, Coerwinkel-Driessen M, van Oost BA, Wieringa B, Ropers HH.
    Genomics; 1989 Oct 01; 5(3):589-95. PubMed ID: 2575588
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  • 16. A long-range restriction map of the human chromosome 19q13 region: close physical linkage between CKMM and the ERCC1 and ERCC2 genes.
    Smeets H, Bachinski L, Coerwinkel M, Schepens J, Hoeijmakers J, van Duin M, Grzeschik KH, Weber CA, de Jong P, Siciliano MJ.
    Am J Hum Genet; 1990 Mar 01; 46(3):492-501. PubMed ID: 2309701
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  • 17. 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 01; 31(1):33-6. PubMed ID: 8151634
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  • 18. Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.
    Johnson K, Nimmo E, Jones P, Weiss M, Savontaus ML, Anvret M, Bartlett R, Roses A, Shaw D, Harper PS.
    Hum Genet; 1988 Dec 01; 80(4):379-81. PubMed ID: 3198115
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  • 19. 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 01; 28(2):89-91. PubMed ID: 2002492
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  • 20. Myotonic dystrophy: update on progress to define the gene.
    Roses AD, Pericak-Vance MA, Bartlett RJ, Yamaoka LH, Lee JE, Koh J, Chen JC, Gilbert JR, Ross DA, Herbstreith MH.
    Aust Paediatr J; 1988 Feb 01; 24 Suppl 1():66-9. PubMed ID: 3060077
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