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Peroxisome Biogenesis Disorder, Complementation Group G

Known as: CGG 
National Institutes of Health

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Broader (1)

Peroxisomal Disorders

Papers overview

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Highly Cited
2011
Highly Cited
2011
Selective executive markers of at-risk profiles associated with the fragile X premutation
Objective: This study determined whether CGG repeat length moderates the relationship between age and performance on selective… 
2010
2010
Effects of race/ethnicity on triple CGG counts in the FMR1 gene in infertile women and egg donors.
Highly Cited
1999
Highly Cited
1999
Expansion and Deletion of Triplet Repeat Sequences inEscherichia coli Occur on the Leading Strand of DNA Replication*
Expansions and deletions of triplet repeat sequences that cause human hereditary neurological diseases were previously suggested… 
Highly Cited
1996
Highly Cited
1996
FMR1 in global populations.
Fragile X syndrome, a frequent form of inherited mental retardation, results from the unstable expansion of a cryptic CGG repeat… 
1996
1996
CTG Triplet Repeats from Human Hereditary Diseases Are Dominant Genetic Expansion Products in Escherichia coli(*)
The relative ability of the 10 triplet repeat sequences to be expanded in Escherichia coli was determined. Surprisingly, CTG… 
Highly Cited
1995
Highly Cited
1995
Instability of the CGG repeat and expression of the FMR1 protein in a male fragile X patient with a lung tumor.
The molecular mechanism of the fragile X syndrome is based on the expansion of an CGG repeat in the 5' UTR of the FMR1 gene in… 
Highly Cited
1994
Highly Cited
1994
Emotional and neurocognitive deficits in fragile X.
We have studied the neurocognitive deficit in premutation and full mutation women as compared to control women and to explore the… 
Highly Cited
1994
Highly Cited
1994
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.
The mutation observed in the fragile X syndrome, an X-linked inherited disorder causing mental retardation, is almost exclusively… 
Highly Cited
1993
Highly Cited
1993
Mental Status and Fragile X Expression in Relation to FMR-1 Gene Mutation
The fragile X mental retardation syndrome is caused by unstable expansion of a CGG repeat in the FMR-1 gene. Clinical expression… 
Highly Cited
1993
Highly Cited
1993
A study of the physical, behavioral, and medical phenotype, including anthropometric measures, of females with fragile X syndrome.
The physical features of fragile X, including a long face, prominent ears, and hyperextensible joints, are present in affected… 
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