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Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.
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    Losekoot M, Hoogendoorn E, Olmer R, et al
    Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.

    Publication history

    • First published November 1, 1997.
    Online issue publication 
    November 01, 1997

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