Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation
- 1 July 1993
- journal article
- research article
- Published by Elsevier BV in Cell
- Vol. 74 (1), 127-134
- https://doi.org/10.1016/0092-8674(93)90300-f
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Vertical Integration of Cosmid and YAC Resources for Interval Mapping on the X-ChromosomeGenomics, 1993
- The identification of a third fragile site, FRAXF, in Xq27 — q28 distal to both FRAXA and FRAXEHuman Molecular Genetics, 1993
- Fragile X founder effect?Nature Genetics, 1992
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 1991
- Chromosomal fragile sitesGenetic Analysis: Biomolecular Engineering, 1991
- Absence of expression of the FMR-1 gene in fragile X syndromeCell, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeCell, 1991
- Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridizationCytogenetic and Genome Research, 1990
- Common fragile sites in man and three closely related primate speciesCytogenetic and Genome Research, 1990
- Fragile sites, telomeric DNA sequences, B chromosomes, and DNA content in raccoon dogs, Nyctereutes procyonoides, with comparative notes on foxes, coyote, wolf, and raccoonCytogenetic and Genome Research, 1988