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

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

Abstract 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...

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Bibliographic Details
Main Authors: Hua Xie, Fang Liu, Yu Zhang, Qian Chen, Shaofang Shangguan, Zhijie Gao, Nan Wu, Jian Wang, Xiaodai Cui, Lin Wang, Xiaoli Chen
Format: Article
Language:English
Published: Wiley 2020-11-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
16p11.2 microdeletion
frequency
neurodevelopmental disorder
neurodevelopmental trajectory
whole‐genome expression profiling
Online Access:https://doi.org/10.1002/mgg3.1485

Internet

https://doi.org/10.1002/mgg3.1485

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