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Q47608194-B8F86824-4115-45C3-A2DF-ACD04ED21749
Q47608194-B8F86824-4115-45C3-A2DF-ACD04ED21749
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Statement
http://www.wikidata.org/entity/statement/Q47608194-B8F86824-4115-45C3-A2DF-ACD04ED21749
Detection of an Underlying 22q11.2 Duplication in a Female Neonate With Trisomy 18.
P2860
Q47608194-B8F86824-4115-45C3-A2DF-ACD04ED21749
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47608194-B8F86824-4115-45C3-A2DF-ACD04ED21749
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wasDerivedFrom
194e772b22dfc764942d682d8a6505479cd8b1d8
P2860
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.