Fragile X syndrome is an important disease of hereditary mental retardation. Its prevalence in the Chinese population is not clear. We amplified FMR1 CGG repeats from male newborns' blood spots. Approximately 45% of the males had 28 CGG repeats and another 19% had 29 repeats. Besides this major peak, there was a second peak at 34 and 35 repeats. From the 1000 males studied, 3 were found to have repeat numbers in the high borderline range (each with 50, 52 and 53 repeats). This result provides a low but significant risk of fragile X syndrome in the Chinese population
Fragile X syndrome (FXS) is the most common inherited intellectual disability. It is caused by the o...
The CGG trinucleotide repeat within the FMR1 gene is associated with multiple clinical disorders, in...
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability (ID) and co-mo...
SUMMARY. The fragile X syndrome is believed to be caused by an expansion of a CGG trinucleotide repe...
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...
with 29 repeats found most common among Malays and Indians while 28 repeats were most common among C...
Based on molecular screening, we estimated the frequencies of fragile X syndrome and FRAXE syndrome ...
The fragile X syndrome is the most common form of inher-ited mental retardation and is mainly due to...
Background: Fragile X syndrome is the most common genetic disorder of intellectual developmental dis...
Fragile X Syndrome (FXS) is the most frequent hereditary form of mental retardation, caused by an ex...
Fragile X Syndrome (FXS) is the most frequent hereditary form of mental retardation, caused by an ex...
The CGG trinucleotide repeat within the FMR1 gene is associated with multiple clinical disorders, in...
If carrier women could be identified in time and take appropriate measures, fragile X syndrome (FXS)...
The CGG trinucleotide repeat within the FMR1 gene is associated with multiple clinical disorders, in...
Fragile X syndrome (FXS) is the most common inherited intellectual disability. It is caused by the o...
The CGG trinucleotide repeat within the FMR1 gene is associated with multiple clinical disorders, in...
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability (ID) and co-mo...
SUMMARY. The fragile X syndrome is believed to be caused by an expansion of a CGG trinucleotide repe...
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...
with 29 repeats found most common among Malays and Indians while 28 repeats were most common among C...
Based on molecular screening, we estimated the frequencies of fragile X syndrome and FRAXE syndrome ...
The fragile X syndrome is the most common form of inher-ited mental retardation and is mainly due to...
Background: Fragile X syndrome is the most common genetic disorder of intellectual developmental dis...
Fragile X Syndrome (FXS) is the most frequent hereditary form of mental retardation, caused by an ex...
Fragile X Syndrome (FXS) is the most frequent hereditary form of mental retardation, caused by an ex...
The CGG trinucleotide repeat within the FMR1 gene is associated with multiple clinical disorders, in...
If carrier women could be identified in time and take appropriate measures, fragile X syndrome (FXS)...
The CGG trinucleotide repeat within the FMR1 gene is associated with multiple clinical disorders, in...
Fragile X syndrome (FXS) is the most common inherited intellectual disability. It is caused by the o...
The CGG trinucleotide repeat within the FMR1 gene is associated with multiple clinical disorders, in...
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability (ID) and co-mo...