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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.
Affiliation
  • 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 ; 48(1): 204, 2022 Dec 29.
Article in En | MEDLINE | ID: mdl-36582000
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome Type of study: Diagnostic_studies / Prognostic_studies Limits: Child, preschool / Humans / Male Language: En Journal: Ital J Pediatr Journal subject: PEDIATRIA Year: 2022 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome Type of study: Diagnostic_studies / Prognostic_studies Limits: Child, preschool / Humans / Male Language: En Journal: Ital J Pediatr Journal subject: PEDIATRIA Year: 2022 Document type: Article Affiliation country: