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Q38794125-2772D784-19DB-45F2-85F2-33F61418604E
Q38794125-2772D784-19DB-45F2-85F2-33F61418604E
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http://www.wikidata.org/entity/statement/Q38794125-2772D784-19DB-45F2-85F2-33F61418604E
Array comparative genomic hybridization and genomic sequencing in the diagnostics of the causes of congenital anomalies.
P2860
Q38794125-2772D784-19DB-45F2-85F2-33F61418604E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38794125-2772D784-19DB-45F2-85F2-33F61418604E
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ccab05a3b6788265a425476d7eecfbc8dbb64acc
P2860
Variants of uncertain significance in newborn screening disorders: implications for large-scale genomic sequencing.