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51. Repeat-primed polymerase chain reaction in myotonic dystrophy type 2 testing. Radvansky J; Ficek A; Kadasi L Genet Test Mol Biomarkers; 2011 Mar; 15(3):133-6. PubMed ID: 21204698 [TBL] [Abstract][Full Text] [Related]
52. [Myotonic dystrophy type 2]. Kimura T Rinsho Shinkeigaku; 2012; 52(11):1267-9. PubMed ID: 23196585 [TBL] [Abstract][Full Text] [Related]
53. PROMM: the expanding phenotype. A family with proximal myopathy, myotonia and deafness. Phillips MF; Rogers MT; Barnetson R; Braun C; Harley HG; Myring J; Stevens D; Wiles CM; Harper PS Neuromuscul Disord; 1998 Oct; 8(7):439-46. PubMed ID: 9829272 [TBL] [Abstract][Full Text] [Related]
54. Report of the 115th ENMC workshop: DM2/PROMM and other myotonic dystrophies. 3rd Workshop, 14-16 February 2003, Naarden, The Netherlands. Udd B; Meola G; Krahe R; Thornton C; Ranum L; Day J; Bassez G; Ricker K Neuromuscul Disord; 2003 Sep; 13(7-8):589-96. PubMed ID: 12921797 [No Abstract] [Full Text] [Related]
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57. Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2. Merlini L; Sabatelli P; Columbaro M; Bonifazi E; Pisani V; Massa R; Novelli G Muscle Nerve; 2005 Jun; 31(6):764-7. PubMed ID: 15704146 [TBL] [Abstract][Full Text] [Related]
58. [A pedigree with myotonic dystrophy: non-CTG, non-CCTG repeat expansion]. Zhao XP; Xie HJ; Zheng HM; Yu ZL; Cui Y; Ding SJ; Ren DM; Tang GM Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):459-62. PubMed ID: 15476170 [TBL] [Abstract][Full Text] [Related]
59. Myotonic dystrophy type 1 (DM1): a triplet repeat expansion disorder. Kumar A; Agarwal S; Agarwal D; Phadke SR Gene; 2013 Jun; 522(2):226-30. PubMed ID: 23570879 [TBL] [Abstract][Full Text] [Related]
60. [Proximal myotonic myopathy (PROMM). Clinical variability within a family]. Eger K; Schulte-Mattler WJ; Zierz S Nervenarzt; 1997 Oct; 68(10):839-44. PubMed ID: 9441258 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]