Neurodevelopmental trajectory and modifiers of 16p11.2 microdeletion: A follow‐up study of four Chinese children carriers

BACKGROUND: Neurodevelopmental disorders (NDDs) are a group of disorders with high genetic and phenotypic heterogeneities. The 16p11.2 microdeletion has been implicated as an important genetic risk factor for NDDs. METHODS: Multiple genetic tests were used to detect the 16p11.2 microdeletion from 91...

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Detalles Bibliográficos
Autores principales: Xie, Hua, Liu, Fang, Zhang, Yu, Chen, Qian, Shangguan, Shaofang, Gao, Zhijie, Wu, Nan, Wang, Jian, Cui, Xiaodai, Wang, Lin, Chen, Xiaoli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667312/
https://www.ncbi.nlm.nih.gov/pubmed/32870608
http://dx.doi.org/10.1002/mgg3.1485

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667312/
https://www.ncbi.nlm.nih.gov/pubmed/32870608
http://dx.doi.org/10.1002/mgg3.1485

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