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Correction: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report

Crossref DOI link: https://doi.org/10.1186/s13052-023-01433-8

Published Online: 2023-03-20

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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