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

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Bibliographic Details
Main Authors: Jinying Wu (Author), Meifang Lei (Author), Xuetao Wang (Author), Nan Liu (Author), Xiaowei Xu (Author), Chunyu Gu (Author), Yuping Yu (Author), Wei Liu (Author)
Format: Book
Published: BMC, 2023-03-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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