139 related articles for article (PubMed ID: 7936256)
21. [Clinical and molecular genetic analyses of congenital myotonic dystrophy].
Kojo T; Arahata K
Nihon Rinsho; 1997 Dec; 55(12):3234-8. PubMed ID: 9436443
[TBL] [Abstract][Full Text] [Related]
22. Discordant clinical outcome in myotonic dystrophy relatives showing (CTG)n > 700 repeats.
Novelli G; Gennarelli M; Menegazzo E; Angelini C; Dallapiccola B
Neuromuscul Disord; 1995 Mar; 5(2):157-9. PubMed ID: 7767095
[TBL] [Abstract][Full Text] [Related]
23. CTG instability in myotonic dystrophy: molecular genetic analysis of families from south-eastern France with characteristics of intergenerational variation in CGT repeat numbers.
Duthel S; Bost M; Ollagnon E; Vial C; Petiot P; Chazot G; Vandenberghe A
Ann Genet; 1999; 42(3):151-9. PubMed ID: 10526658
[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. Somatic cell heterogeneity between DNA extracted from lymphocytes and skeletal muscle in congenital myotonic dystrophy.
Ohya K; Tachi N; Kon S; Kikuchi K; Chiba S
Jpn J Hum Genet; 1995 Dec; 40(4):319-26. PubMed ID: 8851765
[TBL] [Abstract][Full Text] [Related]
26. Myotonic dystrophy gene analysis in affected Israeli families.
Achiron A; Magal N; Shem-Tov N; Noy S; Shohat M; Gadoth N
Isr J Med Sci; 1994 Aug; 30(8):622-5. PubMed ID: 8045745
[TBL] [Abstract][Full Text] [Related]
27. Molecular and clinical characteristics of myotonic dystrophy type 1 in koreans.
Kim SY; Kim JY; Kim GP; Sung JJ; Lim KS; Lee KW; Chae JH; Hong YH; Seong MW; Park SS
Korean J Lab Med; 2008 Dec; 28(6):483-92. PubMed ID: 19127114
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. [Direct genotypic analysis of myotonic dystrophy: detection of an unstable DNA fragment in carriers].
Cobo AM; Martorell L; López de Munain A; Basauri B; Martínez JM; Johnson K; Baiget M
Med Clin (Barc); 1993 Mar; 100(10):361-4. PubMed ID: 8097270
[TBL] [Abstract][Full Text] [Related]
30. Relative stability of a minimal CTG repeat expansion in a large kindred with myotonic dystrophy.
Simmons Z; Thornton CA; Seltzer WK; Richards CS
Neurology; 1998 May; 50(5):1501-4. PubMed ID: 9596022
[TBL] [Abstract][Full Text] [Related]
31. Characteristics of dynamic mutation in Japanese myotonic dystrophy.
Yamagata H; Miki T; Yamanaka N; Takemoto Y; Kanda F; Takahashi K; Inui T; Kinoshita M; Nakagawa M; Higuchi I
Jpn J Hum Genet; 1994 Sep; 39(3):327-35. PubMed ID: 7841443
[TBL] [Abstract][Full Text] [Related]
32. [DNA diagnosis in myotonic dystrophy].
Tachi N
Hokkaido Igaku Zasshi; 1996 Jan; 71(1):3-8. PubMed ID: 8727368
[TBL] [Abstract][Full Text] [Related]
33. Congenital myotonic dystrophy in Britain. II. Genetic basis.
Harper PS
Arch Dis Child; 1975 Jul; 50(7):514-21. PubMed ID: 1167063
[TBL] [Abstract][Full Text] [Related]
34. Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes.
Thornton CA; Johnson K; Moxley RT
Ann Neurol; 1994 Jan; 35(1):104-7. PubMed ID: 8285579
[TBL] [Abstract][Full Text] [Related]
35. Direct molecular analysis of myotonic dystrophy in the German population: important considerations in genetic counselling.
Meiner A; Wolf C; Carey N; Okitsu A; Johnson K; Shelbourne P; Kunath B; Sauermann W; Thiele H; Kupferling P
J Med Genet; 1995 Aug; 32(8):645-9. PubMed ID: 7473660
[TBL] [Abstract][Full Text] [Related]
36. CTG trinucleotide repeat length and clinical expression in a family with myotonic dystrophy.
Takahashi S; Miyamoto A; Oki J; Okuno A
Brain Dev; 1996; 18(2):127-30. PubMed ID: 8733904
[TBL] [Abstract][Full Text] [Related]
37. Molecular diagnosis of homozygous myotonic dystrophy in two asymptomatic sisters.
Cobo A; Martinez JM; Martorell L; Baiget M; Johnson K
Hum Mol Genet; 1993 Jun; 2(6):711-5. PubMed ID: 8353490
[TBL] [Abstract][Full Text] [Related]
38. Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype.
Shelbourne P; Winqvist R; Kunert E; Davies J; Leisti J; Thiele H; Bachmann H; Buxton J; Williamson B; Johnson K
Hum Mol Genet; 1992 Oct; 1(7):467-73. PubMed ID: 1307246
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Delineation of CTG repeats and clinical features in a Taiwanese myotonic dystrophy family.
Jou SB; Lin HM; Pan H; Chiu YL; Li SY; Lee CC; Hsiao KM
Proc Natl Sci Counc Repub China B; 2001 Jan; 25(1):40-4. PubMed ID: 11254171
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
