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  • Molecular assay reagents intended to identify deletions or duplications of the fragile X mental retardation 1 (FMR1) gene, located at chromosome Xq27.3, which encodes the protein synaptic functional regulator FMR1. Genetic variants at this locus have been associated with premature ovarian failure, fragile X tremor/ataxia syndrome, and fragile X syndrome.
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