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23. Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy. Johnson KJ; Jones PJ; Spurr N; Nimmo E; Davies J; Creed H; Weiss M; Williamson R Cytogenet Cell Genet; 1988; 48(1):13-5. PubMed ID: 2460293 [TBL] [Abstract][Full Text] [Related]
25. An STS from a cDNA located in the myotonic dystrophy region (DM) on human chromosome 19q13.3. Lennon GG; Lamerdin J; Lieuallen K; Amemiya C; Aslanidis C; de Jong PJ; Carrano AV Hum Mol Genet; 1992 Jun; 1(3):217. PubMed ID: 1303190 [No Abstract] [Full Text] [Related]
26. [Myotonic dystrophy of Steinert]. Junien C J Genet Hum; 1989 Jan; 37(1):51-4. PubMed ID: 2565953 [TBL] [Abstract][Full Text] [Related]
27. Cloning of the essential myotonic dystrophy region and mapping of the putative defect. Aslanidis C; Jansen G; Amemiya C; Shutler G; Mahadevan M; Tsilfidis C; Chen C; Alleman J; Wormskamp NG; Vooijs M Nature; 1992 Feb; 355(6360):548-51. PubMed ID: 1346925 [TBL] [Abstract][Full Text] [Related]
28. 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 [TBL] [Abstract][Full Text] [Related]
29. Definition of subchromosomal intervals around the myotonic dystrophy locus at 19q. Brunner H; Coerwinkel-Driessen M; Smeets B; Schonk D; Schepens J; Oerlemans F; Hamel B; Ropers H; Wieringa B Prog Clin Biol Res; 1989; 306():107-14. PubMed ID: 2740406 [No Abstract] [Full Text] [Related]
30. [Advances in molecular genetics of myotonic dystrophy]. Yamagata H; Yamanaka N; Miki T; Ogihara T Nihon Rinsho; 1993 Sep; 51(9):2474-80. PubMed ID: 8411731 [TBL] [Abstract][Full Text] [Related]
31. Myotonic dystrophy and autosomal balanced translocation t(2;20)(p21;q11). Fryns JP; Kleczkowska A; Bulcke I; van den Berghe H Clin Genet; 1984 May; 25(5):446-8. PubMed ID: 6723105 [TBL] [Abstract][Full Text] [Related]
32. Molecular analysis of human muscular dystrophies. Davies KE; Forrest S; Smith T; Kenwrick S; Ball S; Dorkins H; Patterson M Muscle Nerve; 1987; 10(3):191-9. PubMed ID: 2882417 [TBL] [Abstract][Full Text] [Related]
33. Genetic and physical demarcation of the locus for dystrophia myotonica. Wieringa B; Brunner H; Hulsebos T; Schonk D; Ropers HH Adv Neurol; 1988; 48():47-69. PubMed ID: 2891258 [No Abstract] [Full Text] [Related]
34. Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy. Buxton J; Shelbourne P; Davies J; Jones C; Van Tongeren T; Aslanidis C; de Jong P; Jansen G; Anvret M; Riley B Nature; 1992 Feb; 355(6360):547-8. PubMed ID: 1346924 [TBL] [Abstract][Full Text] [Related]
35. 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; 41(3):188-94. PubMed ID: 1682238 [TBL] [Abstract][Full Text] [Related]
36. 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; 355(6360):545-6. PubMed ID: 1346923 [TBL] [Abstract][Full Text] [Related]
37. 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 [TBL] [Abstract][Full Text] [Related]