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Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

Breakpoint Cluster RegionFragile X SyndromeMendelian DisorderGenetic DisorderGeneticsFragile X SpectrumMolecular GeneticsDisease Gene IdentificationSystems BiologyMedicineFragile X PremutationLength VariationVariant InterpretationDevelopmental Delay