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In addition, around 8% of individuals with a deletion have a unique or atypical deletion size (i.e., not type I or II) due to various causes, such as unbalanced translocations ( Figure 1 Maternal uniparental disomy (mUPD), where both copies of chromosome 15 come from the mother, is responsible for approximately 35% of PWS cases and results from errors during meiosis

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