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25. Structural organization and developmental expression pattern of the mouse WD-repeat gene DMR-N9 immediately upstream of the myotonic dystrophy locus. Jansen G; Bächner D; Coerwinkel M; Wormskamp N; Hameister H; Wieringa B Hum Mol Genet; 1995 May; 4(5):843-52. PubMed ID: 7633444 [TBL] [Abstract][Full Text] [Related]
26. Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibrium studies in the Japanese population. Yamagata H; Nakagawa M; Johnson K; Miki T J Hum Genet; 1998; 43(4):246-9. PubMed ID: 9852676 [TBL] [Abstract][Full Text] [Related]
27. Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal allele. Hofmann-Radvanyi H; Lavedan C; Rabès JP; Savoy D; Duros C; Johnson K; Junien C Hum Mol Genet; 1993 Aug; 2(8):1263-6. PubMed ID: 7691346 [TBL] [Abstract][Full Text] [Related]
29. Myotonic dystrophy: another case of too many repeats? Shelbourne P; Johnson K Hum Mutat; 1992; 1(3):183-9. PubMed ID: 1301924 [TBL] [Abstract][Full Text] [Related]
30. (CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patients. Novelli G; Gennarelli M; Menegazzo E; Mostacciuolo ML; Pizzuti A; Fattorini C; Tessarolo D; Tomelleri G; Giacanelli M; Danieli GA Biochem Med Metab Biol; 1993 Aug; 50(1):85-92. PubMed ID: 8373638 [TBL] [Abstract][Full Text] [Related]
31. Normal variation at the myotonic dystrophy locus in global human populations. Zerylnick C; Torroni A; Sherman SL; Warren ST Am J Hum Genet; 1995 Jan; 56(1):123-30. PubMed ID: 7825567 [TBL] [Abstract][Full Text] [Related]
32. Physical and genetic characterization of the distal segment of the myotonic dystrophy area on 19q. Jansen G; de Jong PJ; Amemiya C; Aslanidis C; Shaw DJ; Harley HG; Brook JD; Fenwick R; Korneluk RG; Tsilfidis C Genomics; 1992 Jul; 13(3):509-17. PubMed ID: 1639379 [TBL] [Abstract][Full Text] [Related]
33. Effect of artificial (CTG) repeat expansion on the expression of myotonin protein kinase (MtPK) in COS-1 cells. Sasagawa N; Saitoh N; Shimokawa M; Sorimachi H; Maruyama K; Arahata K; Isiura S; Suzuki K Biochim Biophys Acta; 1996 Mar; 1315(2):112-6. PubMed ID: 8608167 [TBL] [Abstract][Full Text] [Related]
35. Myotonic dystrophy type 2: human founder haplotype and evolutionary conservation of the repeat tract. Liquori CL; Ikeda Y; Weatherspoon M; Ricker K; Schoser BG; Dalton JC; Day JW; Ranum LP Am J Hum Genet; 2003 Oct; 73(4):849-62. PubMed ID: 14505273 [TBL] [Abstract][Full Text] [Related]
36. Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms. Bailly J; MacKenzie AE; Leblond S; Korneluk RG Hum Genet; 1991 Mar; 86(5):457-62. PubMed ID: 2016086 [TBL] [Abstract][Full Text] [Related]
37. Triplet repeat sequences in human DNA can be detected by hybridization to a synthetic (5'-CGG-3')17 oligodeoxyribonucleotide. Behn-Krappa A; Mollenhauer J; Doerfler W FEBS Lett; 1993 Nov; 333(3):248-50. PubMed ID: 8224187 [TBL] [Abstract][Full Text] [Related]
38. Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure. Otten AD; Tapscott SJ Proc Natl Acad Sci U S A; 1995 Jun; 92(12):5465-9. PubMed ID: 7777532 [TBL] [Abstract][Full Text] [Related]
40. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member. Brook JD; McCurrach ME; Harley HG; Buckler AJ; Church D; Aburatani H; Hunter K; Stanton VP; Thirion JP; Hudson T Cell; 1992 Feb; 68(4):799-808. PubMed ID: 1310900 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]