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Q35752792-8B1D4D74-9FD6-4874-B548-D3C8B2BE7FC2
Q35752792-8B1D4D74-9FD6-4874-B548-D3C8B2BE7FC2
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http://www.wikidata.org/entity/statement/Q35752792-8B1D4D74-9FD6-4874-B548-D3C8B2BE7FC2
A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
P2860
Q35752792-8B1D4D74-9FD6-4874-B548-D3C8B2BE7FC2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35752792-8B1D4D74-9FD6-4874-B548-D3C8B2BE7FC2
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wasDerivedFrom
f13fe5ad4804b9b72a492690f4f4116875d93b32
P2860
Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size