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Q37692368-00717F32-C79D-4B2D-AFF2-BF6FB0BF0848
Q37692368-00717F32-C79D-4B2D-AFF2-BF6FB0BF0848
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Statement
http://www.wikidata.org/entity/statement/Q37692368-00717F32-C79D-4B2D-AFF2-BF6FB0BF0848
Genome-wide copy number variation analysis in a Chinese autism spectrum disorder cohort.
P2860
Q37692368-00717F32-C79D-4B2D-AFF2-BF6FB0BF0848
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37692368-00717F32-C79D-4B2D-AFF2-BF6FB0BF0848
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Statement
wasDerivedFrom
cd07d5902ac0c36cea8c01d7b235ac2d5068be48
P2860
Recurrent de novo mutations implicate novel genes underlying simplex autism risk