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45. Inheritance and pathogenicity of myotonic dystrophy. Johnson K Mol Cell Biol Hum Dis Ser; 1993; 3():85-110. PubMed ID: 8111546 [No Abstract] [Full Text] [Related]
46. Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q. Friedrich U; Brunner H; Smeets D; Lambermon E; Ropers HH Hum Genet; 1987 Mar; 75(3):291-3. PubMed ID: 2881880 [TBL] [Abstract][Full Text] [Related]
47. The syntenic relationship of proximal mouse chromosome 7 and the myotonic dystrophy gene region on human chromosome 19q. Saunders AM; Seldin MF Genomics; 1990 Feb; 6(2):324-32. PubMed ID: 2307474 [TBL] [Abstract][Full Text] [Related]
48. Myotonic dystrophy with no trinucleotide repeat expansion. Thornton CA; Griggs RC; Moxley RT Ann Neurol; 1994 Mar; 35(3):269-72. PubMed ID: 8122879 [TBL] [Abstract][Full Text] [Related]
49. Myotonic dystrophy associated with hereditary motor and sensory neuropathy. Spaans F; Jennekens FG; Mirandolle JF; Bijlsma JB; de Gast GC Brain; 1986 Dec; 109 ( Pt 6)():1149-68. PubMed ID: 3466660 [TBL] [Abstract][Full Text] [Related]
50. Myotonic dystrophy in a large Sicilian kinship: a case report. Trifiletti R; Parano E; Falsaperla R; Incorpora G Childs Nerv Syst; 1995 Aug; 11(8):453-5. PubMed ID: 7585681 [TBL] [Abstract][Full Text] [Related]
51. Myotonic dystrophy and autosomal balanced translocation t(2;20)(p21;q11). Fryns JP; Kleczkowska A; Bulcke I; van den Berghe H Clin Genet; 1984 May; 25(5):446-8. PubMed ID: 6723105 [TBL] [Abstract][Full Text] [Related]
52. Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy. Huson SM; Meredith AL; Sarfarazi M; Shaw DJ; Compston DA; Harper PS J Med Genet; 1986 Feb; 23(1):55-7. PubMed ID: 3081725 [TBL] [Abstract][Full Text] [Related]
53. Detection of the CTG repeat expansion in congenital myotonic dystrophy. Ohya K; Tachi N; Sato T; Kon S; Kikuchi K; Chiba S Jpn J Hum Genet; 1997 Mar; 42(1):169-80. PubMed ID: 9183996 [TBL] [Abstract][Full Text] [Related]
54. [DNA analysis of a pedigree with myotonic dystrophy in Songjiang county, Shanghai]. Xie H; Zheng H; Zheng S; Deng B; Xu J; Cui Y; Wang Y; Xu Z; Ren D Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Oct; 17(5):319-22. PubMed ID: 11024209 [TBL] [Abstract][Full Text] [Related]
55. Proximal myotonic myopathy: clinical and molecular investigation of a Norwegian family with PROMM. Sun C; Henriksen OA; Tranebjaerg L Clin Genet; 1999 Dec; 56(6):457-61. PubMed ID: 10665666 [TBL] [Abstract][Full Text] [Related]
56. Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms. Bailly J; MacKenzie AE; Leblond S; Korneluk RG Hum Genet; 1991 Mar; 86(5):457-62. PubMed ID: 2016086 [TBL] [Abstract][Full Text] [Related]
57. Anticipation in myotonic dystrophy: a parental-sex-related phenomenon. López de Munain A; Blanco A; Emparanza JI; Martí Massó JF; Cobo A; Basauri B; Martorell L; Baiget M; Martínez Lage JM Neuroepidemiology; 1994; 13(1-2):75-8. PubMed ID: 8190210 [TBL] [Abstract][Full Text] [Related]
58. Myotonic dystrophy phenotype without expansion of (CTG)n repeat: an entity distinct from proximal myotonic myopathy (PROMM)? Abbruzzese C; Krahe R; Liguori M; Tessarolo D; Siciliano MJ; Ashizawa T; Giacanelli M J Neurol; 1996 Oct; 243(10):715-21. PubMed ID: 8923304 [TBL] [Abstract][Full Text] [Related]
59. [Clinico-genetic expression of myotonic dystrophy in Istria]. Ristić S; Marković D; Janko D; Kruzić M Lijec Vjesn; 1989; 111(9-10):301-4. PubMed ID: 2633004 [TBL] [Abstract][Full Text] [Related]
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