CNV profiles of Chinese pediatric patients with developmental disorders-Reference-Cited by-同舟云学术

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CNV profiles of Chinese pediatric patients with developmental disorders

Published:2021-04 Issue:4 Volume:23 Page:669-678
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Yuan Haiming,Shangguan Shaofang,Li Zhengchang,Luo Jingsi,Su Jiasun,Yao Ruen,Zhang Shun,Liang Chen,Chen Qian,Gao Zhijie,Zhu Yanli,Zhang Shujie,Li Wei,Lu Weiliang,Zhang Yu,Xie Hua,Liu Fang,Wang Qingming,Lin Yangyang,Liu Liying,Wang Xiuming,Liang Liyang,Zhong Jianmin,Li Haibo,Qiu Haiyan,Zhang Huifeng,Yan Mei,Mireguli Maimaiti,Liu Yanhui,Zhang Dan,Wang Hongying,Lv Haitao,Xie Bobo,Gui Chunrong,Cui Xiaodai,Zou Liping,Wang Jian,Gusella James F.,Shen Yiping,Chen Xiaoli^ORCID

Funder

the Beijing Natural Science Foundation

National Natural Science Foundation of China

National key research and development program

the Major Research Plan of the Provincial Science and Technology Foundation of Guangxi

Capital Health Research and Development of Special

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/s41436-020-01048-y.pdf

Reference39 articles.

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Comprehensive evaluation of the child with global developmental delays or intellectual disability;Clinical and Experimental Pediatrics;2024-09-15

2. Phenotypic and genetic analysis of children with unexplained neurodevelopmental delay and neurodevelopmental comorbidities in a Chinese cohort using trio-based whole-exome sequencing;Orphanet Journal of Rare Diseases;2024-05-19

3. A cohort study of neurodevelopmental disorders and/or congenital anomalies using high resolution chromosomal microarrays in southern Brazil highlighting the significance of ASD;Scientific Reports;2024-02-14

4. A Cohort Study of Individuals with Neurodevelopmental Disorders and/or Congenital Anomalies Investigated by High- Resolution Chromosomal Microarrays in Southern Brazil: The Significance of Autism Spectrum Disorder;2023-11-14

5. Chromosomal Aberrations in Pediatric Patients With Moderate/Severe Developmental Delay/Intellectual Disability With Abundant Phenotypic Heterogeneities: A Single-Center Study;Pediatric Neurology;2023-10

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