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Up to: Chromosome 13 disorder · Uniparental disomy
Paternal uniparental disomy of chromosome 13
Paternal uniparental disomy of chromosome 13 is an uniparental disomy of paternal origin that most likely does not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only father is a carrier.
This condition has no sub-types.