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2. Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent. Wong LJ; Ashizawa T; Monckton DG; Caskey CT; Richards CS Am J Hum Genet; 1995 Jan; 56(1):114-22. PubMed ID: 7825566 [TBL] [Abstract][Full Text] [Related]
3. Minimal somatic instability of CTG repeat in congenital myotonic dystrophy. Tachi N; Ohya K; Chiba S; Sato T; Kikuchi K Pediatr Neurol; 1995 Jan; 12(1):81-3. PubMed ID: 7748368 [TBL] [Abstract][Full Text] [Related]
4. Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart Registry. Chong-Nguyen C; Wahbi K; Algalarrondo V; Bécane HM; Radvanyi-Hoffman H; Arnaud P; Furling D; Lazarus A; Bassez G; Béhin A; Fayssoil A; Laforêt P; Stojkovic T; Eymard B; Duboc D Circ Cardiovasc Genet; 2017 Jun; 10(3):. PubMed ID: 28611030 [TBL] [Abstract][Full Text] [Related]
5. Surgical repair for atrial septal defect associated with myotonic dystrophy. Ogawa T; Saga T; Nakamoto S Circ J; 2007 Aug; 71(8):1321-2. PubMed ID: 17652903 [TBL] [Abstract][Full Text] [Related]
6. Myotonic dystrophy: an unstable CTG repeat in a protein kinase gene. Timchenko L; Monckton DG; Caskey CT Semin Cell Biol; 1995 Feb; 6(1):13-9. PubMed ID: 7620117 [TBL] [Abstract][Full Text] [Related]
9. Instability of the (CTG)n repeat in congenital myotonic dystrophy. Wong LJ; Ashizawa T Am J Hum Genet; 1997 Dec; 61(6):1445-8. PubMed ID: 9399912 [No Abstract] [Full Text] [Related]
10. A newborn girl with hypotonia and respiratory failure. Charrow J Pediatr Ann; 2007 Dec; 36(12):777, 781-2. PubMed ID: 18229518 [No Abstract] [Full Text] [Related]
11. 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]
12. [Cataract as an only clinical manifestation of myotonic dystrophy--a new example of somatic instability of CTG repeats expansion in myotonin protein kinase gene]. Saito Y; Sato K; Kawai M Rinsho Shinkeigaku; 1997 Aug; 37(8):714-6. PubMed ID: 9404152 [TBL] [Abstract][Full Text] [Related]
13. Transgenic overexpression of human DMPK accumulates into hypertrophic cardiomyopathy, myotonic myopathy and hypotension traits of myotonic dystrophy. O'Cochlain DF; Perez-Terzic C; Reyes S; Kane GC; Behfar A; Hodgson DM; Strommen JA; Liu XK; van den Broek W; Wansink DG; Wieringa B; Terzic A Hum Mol Genet; 2004 Oct; 13(20):2505-18. PubMed ID: 15317754 [TBL] [Abstract][Full Text] [Related]
18. Congenital myotonic dystrophy pathology and somatic mosaicism. Joseph JT; Richards CS; Anthony DC; Upton M; Perez-Atayde AR; Greenstein P Neurology; 1997 Nov; 49(5):1457-60. PubMed ID: 9371942 [TBL] [Abstract][Full Text] [Related]
19. Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? Zatz M; Passos-Bueno MR; Cerqueira A; Marie SK; Vainzof M; Pavanello RC Hum Mol Genet; 1995 Mar; 4(3):401-6. PubMed ID: 7795594 [TBL] [Abstract][Full Text] [Related]
20. Cardiac involvement in a large kindred with myotonic dystrophy. Quantitative assessment and relation to size of CTG repeat expansion. Tokgozoglu LS; Ashizawa T; Pacifico A; Armstrong RM; Epstein HF; Zoghbi WA JAMA; 1995 Sep; 274(10):813-9. PubMed ID: 7650805 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]