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.
26. Incomplete manifestations of myotonic dystrophy in a large kinship in Labrador. Pryse-Phillips W; Johnson GJ; Larsen B Ann Neurol; 1982 Jun; 11(6):582-91. PubMed ID: 6956246 [TBL] [Abstract][Full Text] [Related]
28. Prenatal diagnosis in myotonic dystrophy type 1. Thirteen years of experience: implications for reproductive counselling in DM1 families. Martorell L; Cobo AM; Baiget M; Naudó M; Poza JJ; Parra J Prenat Diagn; 2007 Jan; 27(1):68-72. PubMed ID: 17154336 [TBL] [Abstract][Full Text] [Related]
29. [Expansion and mutation rate in CTG repeats in the myotonic dystrophy gene]. Khidiiatova IM; Fatkhlislamova RI; Magzhanov RV; Popova SN; Slominskiĭ PA; Limborskaia SA; Khusnutdinova EK Genetika; 2000 Oct; 36(10):1410-3. PubMed ID: 11094756 [TBL] [Abstract][Full Text] [Related]
30. Genealogical study of myotonic dystrophy in Istria (Croatia). Medica I; Logar N; Mileta DL; Peterlin B Ann Genet; 2004; 47(2):139-46. PubMed ID: 15183746 [TBL] [Abstract][Full Text] [Related]
31. Unusual clinical, laboratory, and muscle histopathological findings in a family with myotonic dystrophy type 2. Toth C; Dunham C; Suchowersky O; Parboosingh J; Brownell K Muscle Nerve; 2007 Feb; 35(2):259-64. PubMed ID: 17068784 [TBL] [Abstract][Full Text] [Related]
32. [Regional clinico-genetic features of myotonias]. Khannanova FK Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(3):342-6. PubMed ID: 2939672 [TBL] [Abstract][Full Text] [Related]
33. Haplotype analysis of the myotonic dystrophy type 1 (DM1) locus in Taiwan: implications for low prevalence and founder mutations of Taiwanese myotonic dystrophy type 1. Pan H; Lin HM; Ku WY; Li TC; Li SY; Lin CC; Hsiao KM Eur J Hum Genet; 2001 Aug; 9(8):638-41. PubMed ID: 11528511 [TBL] [Abstract][Full Text] [Related]
34. [Ocular findings in patients with Steinert myotonic dystrophy]. Markowska E; Zalewska R; Mariak Z; Wojnar M Przegl Lek; 2006; 63(8):662-3. PubMed ID: 17441379 [TBL] [Abstract][Full Text] [Related]
37. [Cardiological studies on patients with autosomal dominant and autosomal recessive hereditary myotonia congenital and myotonia dystrophica]. Bodem R; Boikhan MS; Kuhn E Verh Dtsch Ges Inn Med; 1971; 77():1289-90. PubMed ID: 5156008 [No Abstract] [Full Text] [Related]
38. [Molecular genetic study in congenital myotonic dystrophy]. Martín P; Sierra J; Losada A; Rufo M; Lucas M Rev Neurol; 1997 Jun; 25(142):833-6. PubMed ID: 9244607 [TBL] [Abstract][Full Text] [Related]