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Q30849515-B0FDC1A2-5486-476F-BDFE-E032E2328268
Q30849515-B0FDC1A2-5486-476F-BDFE-E032E2328268
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http://www.wikidata.org/entity/statement/Q30849515-B0FDC1A2-5486-476F-BDFE-E032E2328268
Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data
P2860
Q30849515-B0FDC1A2-5486-476F-BDFE-E032E2328268
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30849515-B0FDC1A2-5486-476F-BDFE-E032E2328268
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0398affc12c37ab6e6fb9b86396ff55a7600709e
P2860
Identification of small exonic CNV from whole-exome sequence data and application to autism spectrum disorder.