Among the hallmark phenotypes reported in individuals with fragile X syndrome (FXS) are
deficits in attentional function, inhibitory control, and cognitive flexibility, a set of cognitive …

Fragile X syndrome (FXS) is a leading cause of inherited mental retardation. In the vast
majority of cases, this X-linked disorder is due to a CGG expansion in the 5′ untranslated …

Fragile X syndrome (FXS) is the most common inherited form of intellectual disability and
results from the loss of the fragile X mental retardation protein (FMRP). Many fragile X …

Individuals affected by Fragile X syndrome (FXS) experience cognitive impairment,
hyperactivity, attention deficits, social anxiety and autistic-like behaviors. FXS results from …

The fragile X mental retardation protein (FMRP) plays an important role in normal brain
development. Absence of FMRP results in abnormal neuronal morphologies in a selected …

The Fragile X syndrome (FXS) is the most frequent form of inherited mental disability and is
considered a monogenic cause of autism spectrum disorder. FXS is caused by a triplet …

Fragile X Syndrome (FXS) is the most common single gene cause of inherited mental
impairment, and cognitive deficits can range from simple learning disabilities to mental …

Fragile X syndrome (FXS) is caused by a lack of the fragile X mental retardation protein
(FMRP) due to silencing of the Fmr1 gene. As an RNA binding protein, FMRP is thought to …

Fragile X syndrome (FraX) remains the most common inherited cause of intellectual
disability and provides a valuable model for studying gene‐brain‐behavior relationships …

Fragile X syndrome is a neurodevelopmental disorder that is caused by the silencing of a
single gene on the X chromosome, the fragile X mental retardation 1 (FMR1) gene. Affected …