DNA methylation and triplet repeat stability: New proposals addressing actual questions on the CGG repeat of fragile X syndrome
- 9 August 1996
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 64 (2) , 266-267
- https://doi.org/10.1002/ajmg.1320640202
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a causal involvement of methyl-directed DNA mismatch repair in triplet repeat stabilityHuman Molecular Genetics, 1995
- Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instabilityNature Genetics, 1995
- Mismatch Repair, Genetic Stability, and CancerScience, 1994
- Simple repeat DNA is not replicated simplyNature Genetics, 1994
- It was a very good year for DNA repairCell, 1994
- Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytesAnnals of Neurology, 1994
- High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndromeHuman Molecular Genetics, 1993
- Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophyHuman Molecular Genetics, 1993
- A study of DNA methylation in myotonic dystrophy.Journal of Medical Genetics, 1993
- Demethylation of CpG islands in embryonic cellsNature, 1991