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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...
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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
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 |
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