Methylation and mutation patterns in the fragile X syndrome
- 15 April 1992
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 43 (1-2) , 268-278
- https://doi.org/10.1002/ajmg.1320430142
Abstract
Click on the article title to read more.Keywords
This publication has 16 references indexed in Scilit:
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromePublished by Elsevier ,1991
- Isolation of Sequences that Span the Fragile X and Identification of a Fragile X-Related CpG IslandScience, 1991
- Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndromeCell, 1991
- Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresisNature, 1991
- New polymorphic DNA marker close to the fragile site FRAXAGenomics, 1990
- A New DNA Marker Tightly Linked to the Fragile X Locus ( FRAXA )Science, 1989
- The frequency of the fragile X chromosome among schoolchildren in Coventry.Journal of Medical Genetics, 1986
- Prevalence of the fragile‐X syndrome in mentally retarded boys in a Swedish countyAmerican Journal of Medical Genetics, 1986
- A premutation that generates a defect at crossing over explains the inheritance of fragile X mental retardationAmerican Journal of Medical Genetics, 1985
- Fragile Sites on Human Chromosomes: Demonstration of Their Dependence on the Type of Tissue Culture MediumScience, 1977