Fragile X syndrome (FXS) is the most common form of monogenic hereditary cognitive
impairment. FXS patient exhibit a high comorbidity rate with autism spectrum disorders�…

Fragile X syndrome (FXS) is the most common inherited form of mental retardation and a
leading genetic cause of autism. There is increasing evidence in both FXS and other forms�…

Fragile X syndrome (FXS) is a neurodevelopmental disorder characterized by intellectual
disability, sensory hypersensitivity, and high incidences of autism spectrum disorders and�…

Fragile X is the most common known inherited cause of intellectual disability and autism,
and it typically results from transcriptional silencing of FMR1 and loss of the encoded�…

Fragile X syndrome (FXS) is the leading inherited cause of mental retardation and autism
spectrum disorders worldwide. It presents with a distinct behavioral phenotype which�…

Fragile X syndrome (FraX), caused by the loss-of-function of one gene (FMR1), is the most
common inherited form of both mental retardation and autism spectrum disorders. The FMR1�…

Fragile X syndrome (FXS) is the most common inherited form of intellectual disability and the
leading genetic cause of autism. It is associated with the lack of fragile X mental retardation�…

Fragile X mental retardation protein (FMRP) is the product of the fragile X mental retardation
1 gene (FMR1), a gene that—when epigenetically inactivated by a triplet nucleotide repeat�…

Fragile X syndrome (FXS) is a common form of inherited intellectual disability and is one of
the leading known causes of autism. The mutation responsible for FXS is a large expansion�…

Fragile X syndrome (FXS) is an inheritable neuropsychological disease caused by silence of
the fmr1 gene and the deficiency of Fragile X mental retardation protein (FMRP). Patients�…