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FMR1

HGNC ↗

Fragile X syndrome

1 article(s) in the watch · Constitutional genetics

Curated publications

7/10

Extended newborn screening using DNA methylation testing for fragile X syndrome in 17,107 infants.

Fragile X syndrome

Gén.14 July 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.