A novel duplication in the FMR1 gene: implications for molecular analysis in fragile X syndrome and repeat

T Mononen1, H von Koskull, R-L Airaksinen

  • 1Department of Clinical Genetics, Kuopio University Hospital, Kuopio, Finland. tarja.mononen@kuh.fi

Clinical Genetics
|October 10, 2007
PubMed

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