Only two of the fragile sites found in humans (FRAXA and FRAXE) have been associated with a clinical phenotype. In mentally retarded individuals with cytogenetic expression of FRAXA a CGG repeat in the FMR1 gene is amplified. Fragile sites are found in many animal species. We have analyzed the FRAXA region containing the CGG repeat in several different species by PCR amplification. In most mammals this region could be amplified; the number of copies of the repeat is deduced. © 1994 Wiley-Liss, Inc
Fragile X syndrome is the commonest familial form of inherited mental retardation. The molecular def...
The vast majority of individuals with the fragile X syndrome show expanded stretches of CGG repeats ...
Of the seven folate-sensitive fragile sites cloned in the human genome, only two have a proven clini...
textabstractOnly two of the fragile sites found in humans (FRAXA and FRAXE) have been associated wit...
The fragile X syndrome is an X-chromosome-linked dominant disorder with reduced penetrance. It is th...
Fragile X syndrome, a frequent form of inherited mental retardation, results from the unstable expan...
Fragile X syndrome, a frequent form of inherited mental retardation, results from the unstable expan...
The fragile X syndrome is an X-chromosome-linked dominant disorder with reduced penetrance. It is th...
SummaryThe fragile X syndrome is due to the new class of dynamic mutations. It is associated with an...
Five folate-sensitive fragile sites have been characterized at the molecular level (FRAXA, FRAXE, FR...
textabstractThe FMR1 gene contains a CGG repeat present in the 5'-untranslated region which can be u...
SUMMARY. The fragile X syndrome is believed to be caused by an expansion of a CGG trinucleotide repe...
The expansion of CGG repeats in the 5′-untranslated region (5′UTR) of FMR1 gene is the...
The expansion of CGG repeats in the 5′-untranslated region (5′UTR) of FMR1 gene is the...
The fragile X syndrome is the most common form of inher-ited mental retardation and is mainly due to...
Fragile X syndrome is the commonest familial form of inherited mental retardation. The molecular def...
The vast majority of individuals with the fragile X syndrome show expanded stretches of CGG repeats ...
Of the seven folate-sensitive fragile sites cloned in the human genome, only two have a proven clini...
textabstractOnly two of the fragile sites found in humans (FRAXA and FRAXE) have been associated wit...
The fragile X syndrome is an X-chromosome-linked dominant disorder with reduced penetrance. It is th...
Fragile X syndrome, a frequent form of inherited mental retardation, results from the unstable expan...
Fragile X syndrome, a frequent form of inherited mental retardation, results from the unstable expan...
The fragile X syndrome is an X-chromosome-linked dominant disorder with reduced penetrance. It is th...
SummaryThe fragile X syndrome is due to the new class of dynamic mutations. It is associated with an...
Five folate-sensitive fragile sites have been characterized at the molecular level (FRAXA, FRAXE, FR...
textabstractThe FMR1 gene contains a CGG repeat present in the 5'-untranslated region which can be u...
SUMMARY. The fragile X syndrome is believed to be caused by an expansion of a CGG trinucleotide repe...
The expansion of CGG repeats in the 5′-untranslated region (5′UTR) of FMR1 gene is the...
The expansion of CGG repeats in the 5′-untranslated region (5′UTR) of FMR1 gene is the...
The fragile X syndrome is the most common form of inher-ited mental retardation and is mainly due to...
Fragile X syndrome is the commonest familial form of inherited mental retardation. The molecular def...
The vast majority of individuals with the fragile X syndrome show expanded stretches of CGG repeats ...
Of the seven folate-sensitive fragile sites cloned in the human genome, only two have a proven clini...