103 related articles for article (PubMed ID: 8357018)
21. [The RFLP of LDR152/PstI in the Chinese and its application to linkage analysis in a myotonic dystrophy family].
Tan J; Qiu XF; Xue JL; Liu ZD; Li YS; Zai CH
Yi Chuan Xue Bao; 1991; 18(1):6-11. PubMed ID: 1674205
[TBL] [Abstract][Full Text] [Related]
22. [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]
23. Myotonic dystrophy: the correlation of (CTG) repeat length in leucocytes with age at onset is significant only for patients with small expansions.
Hamshere MG; Harley H; Harper P; Brook JD; Brookfield JF
J Med Genet; 1999 Jan; 36(1):59-61. PubMed ID: 9950368
[TBL] [Abstract][Full Text] [Related]
24. Expanding complexity in myotonic dystrophy.
Groenen P; Wieringa B
Bioessays; 1998 Nov; 20(11):901-12. PubMed ID: 9872056
[TBL] [Abstract][Full Text] [Related]
25. Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice.
Gourdon G; Radvanyi F; Lia AS; Duros C; Blanche M; Abitbol M; Junien C; Hofmann-Radvanyi H
Nat Genet; 1997 Feb; 15(2):190-2. PubMed ID: 9020847
[TBL] [Abstract][Full Text] [Related]
26. Genetic mapping of a second myotonic dystrophy locus.
Ranum LP; Rasmussen PF; Benzow KA; Koob MD; Day JW
Nat Genet; 1998 Jun; 19(2):196-8. PubMed ID: 9620781
[TBL] [Abstract][Full Text] [Related]
27. Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM gene.
Sabouri LA; Mahadevan MS; Narang M; Lee DS; Surh LC; Korneluk RG
Nat Genet; 1993 Jul; 4(3):233-8. PubMed ID: 8358430
[TBL] [Abstract][Full Text] [Related]
28. [Myotonic dystrophy of Steinert].
Junien C
J Genet Hum; 1989 Jan; 37(1):51-4. PubMed ID: 2565953
[TBL] [Abstract][Full Text] [Related]
29. [Hereditary diseases affecting muscles].
Kohn A
Harefuah; 1994 Mar; 126(5):276-8. PubMed ID: 8188109
[No Abstract] [Full Text] [Related]
30. Myotonic dystrophy protein kinase gene expression in skeletal muscle from congenitally affected infants.
Laurent A; Costa JM; Assouline B; Voyer M; Vidaud M
Ann Genet; 1997; 40(3):169-74. PubMed ID: 9401107
[TBL] [Abstract][Full Text] [Related]
31. [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]
32. Isolation and ordering of bacteriophage genomic clones corresponding to two YACs from 19q13.3.
Buxton J; Davies J; Shelbourne P; Yokobata K; Williamson R; Johnson K
Mol Cell Probes; 1993 Feb; 7(1):75-80. PubMed ID: 8455645
[TBL] [Abstract][Full Text] [Related]
33. [Medical pathology due to trinucleotide repeats].
Arenas-Aranda D; Peñaloza R; Salamanca-Gómez F
Gac Med Mex; 1999; 135(1):53-65. PubMed ID: 10204311
[TBL] [Abstract][Full Text] [Related]
34. Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1.
Abbruzzese C; Costanzi Porrini S; Mariani B; Gould FK; McAbney JP; Monckton DG; Ashizawa T; Giacanelli M
Ann Neurol; 2002 Oct; 52(4):435-41. PubMed ID: 12325072
[TBL] [Abstract][Full Text] [Related]
35. [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]
36. [The role of trinucleotide repeats in human genetic diseases].
Hietanen K
Duodecim; 1996; 112(3):188-93. PubMed ID: 10590627
[No Abstract] [Full Text] [Related]
37. Anticipation legitimized: unstable DNA to the rescue.
Sutherland GR; Richards RI
Am J Hum Genet; 1992 Jul; 51(1):7-9. PubMed ID: 1609807
[No Abstract] [Full Text] [Related]
38. Genetic epidemiology of myotonic dystrophy.
Mostacciuolo ML; Barbujani G; Armani M; Danieli GA; Angelini C
Genet Epidemiol; 1987; 4(4):289-98. PubMed ID: 3666435
[TBL] [Abstract][Full Text] [Related]
39. An STS from a cDNA located in the myotonic dystrophy region (DM) on human chromosome 19q13.3.
Lennon GG; Lamerdin J; Lieuallen K; Amemiya C; Aslanidis C; de Jong PJ; Carrano AV
Hum Mol Genet; 1992 Jun; 1(3):217. PubMed ID: 1303190
[No Abstract] [Full Text] [Related]
40. Unstable DNA sequence in myotonic dystrophy.
Harley HG; Rundle SA; Reardon W; Myring J; Crow S; Brook JD; Harper PS; Shaw DJ
Lancet; 1992 May; 339(8802):1125-8. PubMed ID: 1349364
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
