Clinical phenotypes study of 231 children with Williams syndrome in China: A single‐center retrospective study

BACKGROUND: Williams syndrome (WS) is a multisystem neurodevelopmental disorder caused by microdeletions in 7q11.23. This study aims to characterize the clinical phenotypes of Chinese children with WS to help for the early diagnosis and intervention of this disease. METHODS: 231 children diagnosed w...

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Detalles Bibliográficos
Autores principales: Li, Fang‐fang, Chen, Wei‐jun, Yao, Dan, Xu, Lin, Shen, Ji‐yang, Zeng, Yan, Shi, Zhuo, Ye, Xiao‐wei, Kang, Dao‐huan, Xu, Bin, Shao, Jie, Ji, Chai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747549/
https://www.ncbi.nlm.nih.gov/pubmed/36168091
http://dx.doi.org/10.1002/mgg3.2069

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747549/
https://www.ncbi.nlm.nih.gov/pubmed/36168091
http://dx.doi.org/10.1002/mgg3.2069

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