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Q38748907-04552C2E-E646-43DF-9254-678E93758C98
Q38748907-04552C2E-E646-43DF-9254-678E93758C98
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http://www.wikidata.org/entity/statement/Q38748907-04552C2E-E646-43DF-9254-678E93758C98
Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders
P2860
Q38748907-04552C2E-E646-43DF-9254-678E93758C98
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38748907-04552C2E-E646-43DF-9254-678E93758C98
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f97313ebe9362cb2f51b446eb273013909e247ff
P2860
Assessing copy number from exome sequencing and exome array CGH based on CNV spectrum in a large clinical cohort.