These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
156 related articles for article (PubMed ID: 2361046)
21. Presymptomatic testing for myotonic dystrophy by means of the linked DNA marker APOC2. Haan EA; Mulley JC; Gedeon AK; Sheffield LJ; Sutherland GR Med J Aust; 1988 Sep; 149(6):326-9. PubMed ID: 3047535 [TBL] [Abstract][Full Text] [Related]
22. 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]
23. Contrasts in clinical presentation and genetic transmission of myotonic dystrophy. Reifer H; Sobel E J Am Podiatr Med Assoc; 1998 Jul; 88(7):313-22. PubMed ID: 9680767 [TBL] [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; 269(15):1960-5. PubMed ID: 8464127 [TBL] [Abstract][Full Text] [Related]
25. Congenital myotonic dystrophy: molecular diagnosis and clinical study. Hojo K; Yamagata H; Moji H; Fujita T; Miki T; Fujimura M; Kidoguchi K Am J Perinatol; 1995 May; 12(3):195-200. PubMed ID: 7612095 [TBL] [Abstract][Full Text] [Related]
26. 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]
27. Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French family. Lucotte G; Berriche S; David F; Mariotti M; Turpin JC Genet Couns; 1994; 5(2):171-4. PubMed ID: 7917127 [TBL] [Abstract][Full Text] [Related]
30. The secretor locus as a marker for prenatal prediction of myotonic dystrophy (DM). Greiner J; Spengler DH; Krüger J; Tariverdian G Hum Genet; 1988 Apr; 78(4):330-2. PubMed ID: 3162894 [TBL] [Abstract][Full Text] [Related]
31. 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; 28(2):84-8. PubMed ID: 1672160 [TBL] [Abstract][Full Text] [Related]
35. Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q. Johnson K; Nimmo E; Jones P; Weiss M; Savontaus ML; Anvret M; Bartlett R; Roses A; Shaw D; Harper PS Hum Genet; 1988 Dec; 80(4):379-81. PubMed ID: 3198115 [TBL] [Abstract][Full Text] [Related]
36. [Myotonic dystrophy]. Nesterov LN; Sushcheva GP; Viatkina SIa; Nesterova IM Zh Nevropatol Psikhiatr Im S S Korsakova; 1983; 83(11):1636-41. PubMed ID: 6232784 [TBL] [Abstract][Full Text] [Related]
37. The myotonic dystrophies: diagnosis and management. Turner C; Hilton-Jones D J Neurol Neurosurg Psychiatry; 2010 Apr; 81(4):358-67. PubMed ID: 20176601 [TBL] [Abstract][Full Text] [Related]
38. [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]