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  • Molecular assay reagents intended for use in identifying the abnormal situation in which both members of the chromosome pair 11 are inherited from the father (i.e., uniparental disomy [UPD]) and the mother\'s chromosome for that pair is missing (i.e., UPD of chromosome 11). Paternally inherited disomy 11 is associated with Beckwith-Wiedemann syndrome (BWS).
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