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Q21091190-B6B5D2F2-2E28-40A1-A3FA-CA2DE952E7AE
Q21091190-B6B5D2F2-2E28-40A1-A3FA-CA2DE952E7AE
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http://www.wikidata.org/entity/statement/Q21091190-B6B5D2F2-2E28-40A1-A3FA-CA2DE952E7AE
Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome
P2860
Q21091190-B6B5D2F2-2E28-40A1-A3FA-CA2DE952E7AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21091190-B6B5D2F2-2E28-40A1-A3FA-CA2DE952E7AE
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wasDerivedFrom
adedb0473adbef0025399e6d0003d0a5c5218e8d
P2860
Molecular characterization of de novo secondary trisomy 13.