Modeling the natural history of the fragile X gene
- 1 January 1995
- journal article
- Published by Wiley in Mental Retardation and Developmental Disabilities Research Reviews
- Vol. 1 (4) , 263-268
- https://doi.org/10.1002/mrdd.1410010406
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Precursor arrays for triplet repeat expansion at the fragile X locusHuman Molecular Genetics, 1994
- Sequence analysis of the fragile X trinucleotide repeat: implications for the origin of the fragile X mutationHuman Molecular Genetics, 1994
- Population genetics of fragile X: A multiple allele model with variable risk of CGG repeat expansionAmerican Journal of Medical Genetics, 1994
- Insert size and flanking haplotype in fragile X and normal populations: possible multiple origins for the fragile X mutationHuman Molecular Genetics, 1994
- Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradoxCell, 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 syndromePublished by Elsevier ,1991
- Preventive Screening for the Fragile X SyndromeNew England Journal of Medicine, 1986
- Further segregation analysis of the fragile X syndrome with special reference to transmitting malesHuman Genetics, 1985
- The marker (X) syndrome: a cytogenetic and genetic analysisAnnals of Human Genetics, 1984