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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.
Wu, Jinying; Lei, Meifang; Wang, Xuetao; Liu, Nan; Xu, Xiaowei; Gu, Chunyu; Yu, Yuping; Liu, Wei.
Afiliação
  • Wu J; Tianjin Pediatric Research Institute, Tianjin Children's Hospital (Children's Hospital of Tianjin University), Tianjin, 300134, China.
  • Lei M; Tianjin Key Laboratory of Birth Defects for Prevention and Treatment, Tianjin, 300134, China.
  • Wang X; Department of Neurology, Tianjin Children's Hospital (Children's Hospital of Tianjin University), Tianjin, 300134, China.
  • Liu N; Tianjin Pediatric Research Institute, Tianjin Children's Hospital (Children's Hospital of Tianjin University), Tianjin, 300134, China.
  • Xu X; Tianjin Key Laboratory of Birth Defects for Prevention and Treatment, Tianjin, 300134, China.
  • Gu C; Tianjin Pediatric Research Institute, Tianjin Children's Hospital (Children's Hospital of Tianjin University), Tianjin, 300134, China.
  • Yu Y; Tianjin Key Laboratory of Birth Defects for Prevention and Treatment, Tianjin, 300134, China.
  • Liu W; Tianjin Pediatric Research Institute, Tianjin Children's Hospital (Children's Hospital of Tianjin University), Tianjin, 300134, China.
Ital J Pediatr ; 49(1): 32, 2023 Mar 20.
Article em En | MEDLINE | ID: mdl-36941634
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article