Reverse mutations in the fragile X syndrome
- 9 August 1996
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics
- Vol. 64 (2) , 287-292
- https://doi.org/10.1002/(sici)1096-8628(19960809)64:2<287::aid-ajmg11>3.0.co;2-b
Abstract
No abstract availableKeywords
This publication has 34 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
- A complex mutable polymorphism located within the fragile X geneNature Genetics, 1993
- Characterization of a highly polymorphic dinucleotide repeat 150 KB proximal to the fragile X siteAmerican Journal of Medical Genetics, 1992
- Prenatal detection of Fra(X)(q27.3) in female identical twins: Reliability of low level cytogenetic prenatal expression in femalesAmerican Journal of Medical Genetics, 1992
- Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.Journal of Medical Genetics, 1991
- 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
- Further segregation analysis of the fragile X syndrome with special reference to transmitting malesHuman Genetics, 1985