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22. Distribution and evolution of CTG repeats at the myotonin protein kinase gene in human populations. Deka R; Majumder PP; Shriver MD; Stivers DN; Zhong Y; Yu LM; Barrantes R; Yin SJ; Miki T; Hundrieser J; Bunker CH; McGarvey ST; Sakallah S; Ferrell RE; Chakraborty R Genome Res; 1996 Feb; 6(2):142-54. PubMed ID: 8919693 [TBL] [Abstract][Full Text] [Related]
23. The lower incidence of myotonic dystrophy in Ashkenazic Jews compared to North African Jews is associated with a significantly lower number of CTG trinucleotide repeats. Mor-Cohen R; Magal N; Gadoth N; Achiron A; Shohat T; Shohat M Isr J Med Sci; 1997 Mar; 33(3):190-3. PubMed ID: 9313789 [TBL] [Abstract][Full Text] [Related]
24. Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy. Ashizawa T; Monckton DG; Vaishnav S; Patel BJ; Voskova A; Caskey CT Genomics; 1996 Aug; 36(1):47-53. PubMed ID: 8812415 [TBL] [Abstract][Full Text] [Related]
25. CTG repeat number at the myotonic dystrophy locus in healthy Kuwaiti individuals: possible explanation of why myotonic dystrophy is rare in Kuwait. Alfadhli S; Elshafey AE; Bastaki L; Al-Awadi S Arch Neurol; 2004 Jun; 61(6):895-8. PubMed ID: 15210527 [TBL] [Abstract][Full Text] [Related]
26. 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 [TBL] [Abstract][Full Text] [Related]
27. Relative stability of a minimal CTG repeat expansion in a large kindred with myotonic dystrophy. Simmons Z; Thornton CA; Seltzer WK; Richards CS Neurology; 1998 May; 50(5):1501-4. PubMed ID: 9596022 [TBL] [Abstract][Full Text] [Related]
28. Instability of normal (CTG)n alleles in the DM kinase gene. Dow DJ; Rubinsztein DC; Yates JR; Barton DE; Ferguson-Smith MA J Med Genet; 1997 Oct; 34(10):871-3. PubMed ID: 9350827 [TBL] [Abstract][Full Text] [Related]
30. Short tandem-repeat polymorphism/alu haplotype variation at the PLAT locus: implications for modern human origins. Tishkoff SA; Pakstis AJ; Stoneking M; Kidd JR; Destro-Bisol G; Sanjantila A; Lu RB; Deinard AS; Sirugo G; Jenkins T; Kidd KK; Clark AG Am J Hum Genet; 2000 Oct; 67(4):901-25. PubMed ID: 10986042 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. Association of CTG repeats and the 1-kb Alu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation. Yamagata H; Miki T; Nakagawa M; Johnson K; Deka R; Ogihara T Hum Genet; 1996 Feb; 97(2):145-7. PubMed ID: 8566943 [TBL] [Abstract][Full Text] [Related]
33. Absence of myotonic dystrophy in southern African Negroids is associated with a significantly lower number of CTG trinucleotide repeats. Goldman A; Ramsay M; Jenkins T J Med Genet; 1994 Jan; 31(1):37-40. PubMed ID: 8151635 [TBL] [Abstract][Full Text] [Related]
34. 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]
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36. Prevalence of myotonic dystrophy in Israeli Jewish communities: inter-community variation and founder premutations. Segel R; Silverstein S; Lerer I; Kahana E; Meir R; Sagi M; Zilber N; Korczyn AD; Shapira Y; Argov Z; Abeliovich D Am J Med Genet A; 2003 Jun; 119A(3):273-8. PubMed ID: 12784291 [TBL] [Abstract][Full Text] [Related]
37. Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission. O'Hoy KL; Tsilfidis C; Mahadevan MS; Neville CE; Barceló J; Hunter AG; Korneluk RG Science; 1993 Feb; 259(5096):809-12. PubMed ID: 8094260 [TBL] [Abstract][Full Text] [Related]
38. Ancestral Origin of the First Indian Families with Myotonic Dystrophy Type 2. Damen M; Schijvenaars M; Schimmel-Naber M; Groothuismink J; Coenen M; Tieleman A J Neuromuscul Dis; 2021; 8(4):715-722. PubMed ID: 34024776 [TBL] [Abstract][Full Text] [Related]
39. Characterization of large CTG repeat expansions in myotonic dystrophy alleles using PCR. Cheng S; Barceló JM; Korneluk RG Hum Mutat; 1996; 7(4):304-10. PubMed ID: 8723679 [TBL] [Abstract][Full Text] [Related]
40. Dynamic balance of segregation distortion and selection maintains normal allele sizes at the myotonic dystrophy locus. Polański A; Chakraborty R; Kimmel M; Deka R Math Biosci; 1998 Jan; 147(1):93-112. PubMed ID: 9401353 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]