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SREP44155
SREP44155
http://dx.doi.org/10.1038/SREP44155
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.
P356
Q37692368-DB797C2F-6E08-4102-B778-5B0A8E2DEF35
P356
SREP44155
http://dx.doi.org/10.1038/SREP44155