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

Detalles Bibliográficos
Autores principales: Wu, Jinying, Lei, Meifang, Wang, Xuetao, Liu, Nan, Xu, Xiaowei, Gu, Chunyu, Yu, Yuping, Liu, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Correction
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029287/
https://www.ncbi.nlm.nih.gov/pubmed/36941634
http://dx.doi.org/10.1186/s13052-023-01433-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10029287/
https://www.ncbi.nlm.nih.gov/pubmed/36941634
http://dx.doi.org/10.1186/s13052-023-01433-8

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