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Journal Abstract Search

118 related items for PubMed ID: 1980487

  • 21. 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]

  • 22. Molecular analysis for the myotonic dystrophy mutation in neuromuscular disorders.
    MacMillan JC, Myring J, Harley HG, Reardon W, Harper PS, Shaw DJ.
    Neuromuscul Disord; 1992 Aug 01; 2(5-6):405-11. PubMed ID: 1363747
    [Abstract] [Full Text] [Related]

  • 23. Triplet-primed PCR is more sensitive than southern blotting-long PCR for the diagnosis of myotonic dystrophy type1.
    Addis M, Serrenti M, Meloni C, Cau M, Melis MA.
    Genet Test Mol Biomarkers; 2012 Dec 01; 16(12):1428-31. PubMed ID: 23030650
    [Abstract] [Full Text] [Related]

  • 24. Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.
    Redman JB, Fenwick RG, Fu YH, Pizzuti A, Caskey CT.
    JAMA; 1993 Apr 21; 269(15):1960-5. PubMed ID: 8464127
    [Abstract] [Full Text] [Related]

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  • 26. 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 21; 24(2):287-94. PubMed ID: 11216395
    [Abstract] [Full Text] [Related]

  • 27. A molecular protocol for diagnosing myotonic dystrophy.
    Guida M, Marger RS, Papp AC, Snyder PJ, Sedra MS, Kissel JT, Mendell JR, Prior TW.
    Clin Chem; 1995 Jan 21; 41(1):69-72. PubMed ID: 7813083
    [Abstract] [Full Text] [Related]

  • 28. Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophy.
    Nokelainen PT, Alanen-Kurki L, Somer HV, Pihko SH, Peltonen L.
    Muscle Nerve; 1991 May 21; 14(5):451-6. PubMed ID: 1678492
    [Abstract] [Full Text] [Related]

  • 29. Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy.
    Harley HG, Brook JD, Rundle SA, Crow S, Reardon W, Buckler AJ, Harper PS, Housman DE, Shaw DJ.
    Nature; 1992 Feb 06; 355(6360):545-6. PubMed ID: 1346923
    [Abstract] [Full Text] [Related]

  • 30. High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation.
    Neville CE, Mahadevan MS, Barceló JM, Korneluk RG.
    Hum Mol Genet; 1994 Jan 06; 3(1):45-51. PubMed ID: 7909252
    [Abstract] [Full Text] [Related]

  • 31. Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q.
    Friedrich U, Brunner H, Smeets D, Lambermon E, Ropers HH.
    Hum Genet; 1987 Mar 06; 75(3):291-3. PubMed ID: 2881880
    [Abstract] [Full Text] [Related]

  • 32. 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 06; 5(4):746-51. PubMed ID: 2591962
    [Abstract] [Full Text] [Related]

  • 33. Molecular analysis of the CTG trinucleotide repeat in South African myotonic dystrophy families--implications for diagnosis and counselling.
    Goldman A, Ramsay M, Jenkins T.
    S Afr Med J; 1995 Nov 06; 85(11):1161-4. PubMed ID: 8597005
    [Abstract] [Full Text] [Related]

  • 34. Identification of variable simple sequence motifs in 19q13.2-qter: markers for the myotonic dystrophy locus.
    Smeets HJ, Hermens R, Brunner HG, Ropers HH, Wieringa B.
    Genomics; 1991 Feb 06; 9(2):257-63. PubMed ID: 1840564
    [Abstract] [Full Text] [Related]

  • 35. 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 06; 28(2):84-8. PubMed ID: 1672160
    [Abstract] [Full Text] [Related]

  • 36. 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 06; 85(3):305-10. PubMed ID: 1975560
    [Abstract] [Full Text] [Related]

  • 37. Significance of mitochondrial DNA deletions in myotonic dystrophy.
    Thyagarajan D, Byrne E, Noer S, Lertrit P, Utthanophol P, Kapsa R, Marzuki S.
    Acta Neurol Scand; 1993 Jan 06; 87(1):32-6. PubMed ID: 8093820
    [Abstract] [Full Text] [Related]

  • 38. Linkage between a muscle-specific CK gene marker and VO2max in the HERITAGE Family Study.
    Rivera MA, Pérusse L, Simoneau JA, Gagnon J, Dionne FT, Leon AS, Skinner JS, Wilmore JH, Province M, Rao DC, Bouchard C.
    Med Sci Sports Exerc; 1999 May 06; 31(5):698-701. PubMed ID: 10331890
    [Abstract] [Full Text] [Related]

  • 39. Molecular diagnosis of homozygous myotonic dystrophy in two asymptomatic sisters.
    Cobo A, Martinez JM, Martorell L, Baiget M, Johnson K.
    Hum Mol Genet; 1993 Jun 06; 2(6):711-5. PubMed ID: 8353490
    [Abstract] [Full Text] [Related]

  • 40. Molecular analysis of two pre-mutations in myotonic dystrophy.
    Yamagata H, Kinoshita M, Komori T, Kondo I, Miki T.
    Clin Genet; 1998 Oct 06; 54(4):354-7. PubMed ID: 9831350
    [Abstract] [Full Text] [Related]

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