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DDV146
DDV146
http://dx.doi.org/10.1093/HMG/DDV146
Alu-mediated diverse and complex pathogenic copy-number variants within human chromosome 17 at p13.3.
P356
Q35766412-92D2D65F-3DD8-4F9B-9B68-6819705F19AF
P356
DDV146
http://dx.doi.org/10.1093/HMG/DDV146