SummaryWe examined premutation-female transmissions and premutation-male transmissions of the FMR1 CGG repeat to carrier offspring, to identify factors associated with instability of the repeat. First we investigated associations between parental and offspring repeat size. Premutation-female repeat size was positively correlated with the risk of having full-mutation offspring, confirming previous reports. Similarly, premutation-male repeat size was positively correlated with the daughter's repeat size. However, increasing paternal repeat size was associated also with both increased risk of contraction and decreased magnitude of the repeat-size change passed to the daughter. We hypothesized that the difference between the female and male tra...
BACKGROUND: The fragile X premutation is characterized by a large CGG repeat track (55–199 repeats) ...
Myotonic dystrophy type 1 (DM1) is caused by a CTG trinucleotide repeat expansion on chromosome 19q1...
Myotonic dystrophy type 1 (DM1) is caused by a CTG trinucleotide repeat expansion on chromosome 19q1...
SummaryWe examined premutation-female transmissions and premutation-male transmissions of the FMR1 C...
Fragile X syndrome, a form of X-linked mental retardation, results from the hyperexpansion of a CGG ...
BACKGROUND: The presence of AGG interruptions in the CGG repeat locus of the fragile X mental retar...
BACKGROUND: The presence of AGG interruptions in the CGG repeat locus of the fragile X mental retard...
BackgroundThe presence of AGG interruptions in the CGG repeat locus of the fragile X mental retardat...
Fragile X syndrome, a form of X-linked mental retardation, results from the hyperexpansion of a CGG ...
SummaryTo determine the meiotic instability of the CGG-triplet repeat in the fragile-X gene, FMR1, w...
I. AbstractAllele instability in trinucleotides repeat disorders has been associated with many diffe...
Prevalence of the disease in both its full mutation and premutation states was estimated. Confirmat...
Fragile X syndrome is the commonest familial form of inherited mental retardation. The molecular def...
Fragile X Syndrome is caused by the expansion of an unstable CGG-repeat tract in the 5′-UTR of the F...
BACKGROUND: The fragile X premutation is characterized by a large CGG repeat track (55–199 repeats) ...
BACKGROUND: The fragile X premutation is characterized by a large CGG repeat track (55–199 repeats) ...
Myotonic dystrophy type 1 (DM1) is caused by a CTG trinucleotide repeat expansion on chromosome 19q1...
Myotonic dystrophy type 1 (DM1) is caused by a CTG trinucleotide repeat expansion on chromosome 19q1...
SummaryWe examined premutation-female transmissions and premutation-male transmissions of the FMR1 C...
Fragile X syndrome, a form of X-linked mental retardation, results from the hyperexpansion of a CGG ...
BACKGROUND: The presence of AGG interruptions in the CGG repeat locus of the fragile X mental retar...
BACKGROUND: The presence of AGG interruptions in the CGG repeat locus of the fragile X mental retard...
BackgroundThe presence of AGG interruptions in the CGG repeat locus of the fragile X mental retardat...
Fragile X syndrome, a form of X-linked mental retardation, results from the hyperexpansion of a CGG ...
SummaryTo determine the meiotic instability of the CGG-triplet repeat in the fragile-X gene, FMR1, w...
I. AbstractAllele instability in trinucleotides repeat disorders has been associated with many diffe...
Prevalence of the disease in both its full mutation and premutation states was estimated. Confirmat...
Fragile X syndrome is the commonest familial form of inherited mental retardation. The molecular def...
Fragile X Syndrome is caused by the expansion of an unstable CGG-repeat tract in the 5′-UTR of the F...
BACKGROUND: The fragile X premutation is characterized by a large CGG repeat track (55–199 repeats) ...
BACKGROUND: The fragile X premutation is characterized by a large CGG repeat track (55–199 repeats) ...
Myotonic dystrophy type 1 (DM1) is caused by a CTG trinucleotide repeat expansion on chromosome 19q1...
Myotonic dystrophy type 1 (DM1) is caused by a CTG trinucleotide repeat expansion on chromosome 19q1...