We have cloned the fragile site FRAXE and demonstrate that individuals with this fragile site possess amplifications of a GCC repeat adjacent to a CpG island in Xq28 of the human X chromosome. Normal individuals have 6-25 copies of the GCC repeat, whereas mentally retarded, FRAXE-positive individuals have > 200 copies and also have methylation at the CpG island. This situation is similar to that seen at the FRAXA locus and is another example in which a trinucleotide repeat expansion is associated with a human genetic disorder. In contrast with the fragile X syndrome, the GCC repeat can expand or contract and is equally unstable when passed through the male or female line. These results also have implications for the understanding of chro...
The human genome segment upstream of the FMR1 (fragile X mental retardation 1) gene (Xq27.3) contain...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
The human genome segment upstream of the FMR1 (fragile X mental retardation 1) gene (Xq27.3) contain...
We have recently shown that the expression of the FRAXE fragile site in Xq28 is associated with the ...
Expansion of a polymorphic GCC-repeat at the FRAXE locus has been associated with expression of chro...
Expansion of a polymorphic GCC-repeat at the FRAXE locus has been associated with expression of chro...
Three folate-sensitive fragile sites, termed FRAXA, FRAXE and FRAXF, have been identified on the dis...
The FRAXE fragile site, 600 Kb distal to the more common FRAXA, has been reported to be expressed in...
In its expanded form, the fragile X triplet repeat at Xq27.3 gives rise to the most common form of i...
The cytogenetic expression of the folate sensitive fragile site, FRAXE, is due to the expansion of a...
The human genome contains many repeated DNA sequences that vary in complexity of repeating unit from...
Most of the rare folate sensitive fragile sites cloned to date arise from expansion of a CGG:CCG tri...
I. AbstractAllele instability in trinucleotides repeat disorders has been associated with many diffe...
FRAXE mental retardation is a form of mild to moderate intellectual disability generally associated ...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
The human genome segment upstream of the FMR1 (fragile X mental retardation 1) gene (Xq27.3) contain...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
The human genome segment upstream of the FMR1 (fragile X mental retardation 1) gene (Xq27.3) contain...
We have recently shown that the expression of the FRAXE fragile site in Xq28 is associated with the ...
Expansion of a polymorphic GCC-repeat at the FRAXE locus has been associated with expression of chro...
Expansion of a polymorphic GCC-repeat at the FRAXE locus has been associated with expression of chro...
Three folate-sensitive fragile sites, termed FRAXA, FRAXE and FRAXF, have been identified on the dis...
The FRAXE fragile site, 600 Kb distal to the more common FRAXA, has been reported to be expressed in...
In its expanded form, the fragile X triplet repeat at Xq27.3 gives rise to the most common form of i...
The cytogenetic expression of the folate sensitive fragile site, FRAXE, is due to the expansion of a...
The human genome contains many repeated DNA sequences that vary in complexity of repeating unit from...
Most of the rare folate sensitive fragile sites cloned to date arise from expansion of a CGG:CCG tri...
I. AbstractAllele instability in trinucleotides repeat disorders has been associated with many diffe...
FRAXE mental retardation is a form of mild to moderate intellectual disability generally associated ...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
The human genome segment upstream of the FMR1 (fragile X mental retardation 1) gene (Xq27.3) contain...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
The human genome segment upstream of the FMR1 (fragile X mental retardation 1) gene (Xq27.3) contain...