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Q37704614-9444F18E-D604-4A18-86EB-C34F7596B553
Q37704614-9444F18E-D604-4A18-86EB-C34F7596B553
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Statement
http://www.wikidata.org/entity/statement/Q37704614-9444F18E-D604-4A18-86EB-C34F7596B553
The clinical context of copy number variation in the human genome.
P2860
Q37704614-9444F18E-D604-4A18-86EB-C34F7596B553
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37704614-9444F18E-D604-4A18-86EB-C34F7596B553
rank
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wasDerivedFrom
09ff58f6b9c143745d86772682f516c51dc400a7
P2860
Clinical utility of array comparative genomic hybridization: uncovering tumor susceptibility in individuals with developmental delay