Clinical and molecular features of children with Beckwith-Wiedemann syndrome in China: a single-center retrospective cohort study

BACKGROUND: Beckwith-Wiedemann syndrome (BWS) is a genetic overgrowth disorder with variable clinical features and cancer predisposition. In this study, we aim to characterize the clinical features and molecular defects of BWS patients in China. METHODS: Thirty-one patients with clinical suspicion o...

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Detalles Bibliográficos
Autores principales: Wang, Ruixue, Xiao, Yongmei, Li, Dan, Hu, Hui, Li, Xiaolu, Ge, Ting, Yu, Ronghua, Wang, Yizhong, Zhang, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7191772/
https://www.ncbi.nlm.nih.gov/pubmed/32349794
http://dx.doi.org/10.1186/s13052-020-0819-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7191772/
https://www.ncbi.nlm.nih.gov/pubmed/32349794
http://dx.doi.org/10.1186/s13052-020-0819-3

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