Introduction The neurodevelopmental disorder fragile X syndrome (FXS) is the most
common monogenic cause of intellectual disability associated with autism spectrum�…

Fragile X Syndrome (FXS) is the most common form of inherited intellectual disability,
caused by developmentally regulated inactivation of FMR1, leading to the absence of its�…

Human stem and progenitor cells offer an innovative way to study early events in
development. An exciting new opportunity for these cells is their application to study the�…

Patients with fragile X syndrome (FXS) exhibit moderate to severe intellectual disabilities. In
addition, one-third of FXS patients show characteristics of autism spectrum disorder. FXS is�…

Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and is
closely linked with autism. The genetic basis of FXS is an expansion of CGG repeats in the�…

Fragile X syndrome (FXS), the most common form of inherited mental retardation, is a
neurodevelopmental disorder caused by silencing of the FMR1 gene, which in FXS�…

Fragile X syndrome (FXS) is the most common inherited cause of intellectual disability. In
addition to cognitive deficits, FXS patients exhibit hyperactivity, attention deficits, social�…

Abstract Fragile X Syndrome (FXS), the leading monogenic cause of intellectual disability
and autism spectrum disorder, is caused by expansion of a CGG trinucleotide repeat in the�…

Fragile X syndrome (FXS) is a neurodevelopmental disorder, characterized by intellectual
disability and sensory deficits, caused by epigenetic silencing of the FMR1 gene and�…

Fragile X syndrome (FXS) is caused by transcriptional silencing of the FMR1 gene during
embryonic development with the consequent loss of the encoded fragile X mental�…