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  • Molecular assay reagents intended for use in identifying the abnormal situation in which both members of the chromosome pair 14 are inherited from the father (i.e., uniparental disomy [UPD]) and the mother\'s chromosome for that pair is missing. Paternally inherited disomy 14 is characterized by developmental disability, skeletal abnormalities that result in short-limb dwarfism with narrow thorax, decreased survival due to respiratory difficulties, dysmorphic facies, and scoliosis.
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