A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease

被引：0
作者：
Xiaoqing Zhang
Yuejuan Xu
Deyuan Liu
Juan Geng
Sun Chen
Zhengwen Jiang
Qihua Fu
Kun Sun
机构：
[1] Shanghai Jiao Tong University School of Medicine,Department of Laboratory Medicine, Shanghai Children’s Medical Center
[2] Shanghai Jiao Tong University School of Medicine,Department of Pediatric Cardiology, Xinhua Hospital
[3] Genesky Diagnostics (Suzhou) Inc,undefined
来源：
BMC Genomics | / 16卷
关键词：
Copy number variation; 22q11.2 deletion; Congenital heart disease; Multiplex ligation-dependent probe amplification;
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