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Q38866800-BEFAC520-E545-41D0-BF41-B54EB6CE4EBB
Q38866800-BEFAC520-E545-41D0-BF41-B54EB6CE4EBB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38866800-BEFAC520-E545-41D0-BF41-B54EB6CE4EBB
Variants of uncertain significance in newborn screening disorders: implications for large-scale genomic sequencing.
P2860
Q38866800-BEFAC520-E545-41D0-BF41-B54EB6CE4EBB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38866800-BEFAC520-E545-41D0-BF41-B54EB6CE4EBB
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type
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Statement
wasDerivedFrom
4551550cd2afece57094b1f9807dca6a3a1c8bce
P2860
Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates.