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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
Title: Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report.
Authors: Wu, Jinying1,2 (AUTHOR), Lei, Meifang3 (AUTHOR), Wang, Xuetao1,2 (AUTHOR), Liu, Nan1,2 (AUTHOR), Xu, Xiaowei1,2 (AUTHOR), Gu, Chunyu1,2 (AUTHOR), Yu, Yuping4 (AUTHOR), Liu, Wei5 (AUTHOR) lance_1971@163.com
Source: Italian Journal of Pediatrics. 12/29/2022, Vol. 48 Issue 1, p1-7. 7p.
Database: Academic Search Ultimate
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Description
ISSN:17208424
DOI:10.1186/s13052-022-01398-0