[Analysis of de novo copy number variations in a family affected with autism spectrum disorders using high-resolution array-based comparative genomic hybridization].
He, Wen-zhi; Liu, Wei-qiang; Zhong, Xin-qi; Chen, Xiao-lin; Li, Shao-ying; Zhang, Hui-min; Li, Qing; Cui, Qi-liang; Sun, Xiao-fang.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
; 29(3): 266-9, 2012 Jun.
Artigo em Chinês | MEDLINE | ID: mdl-22678785
The genetics of Autism Spectrum Disorders--a guide for clinicians.
Copy number variation characteristics in subpopulations of patients with autism spectrum disorders.
Fenotipo en pacientes con discapacidad intelectual y array-CGH patológico
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Piecewise-constant and low-rank approximation for identification of recurrent copy number variations.
Identification and molecular characterization of two novel chromosomal deletions associated with autism.
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