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
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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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