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Q21091190-8C620E17-F31D-4557-B910-36EB918B6B87
Q21091190-8C620E17-F31D-4557-B910-36EB918B6B87
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21091190-8C620E17-F31D-4557-B910-36EB918B6B87
Small deletions of SATB2 cause some of the clinical features of the 2q33.1 microdeletion syndrome
P2860
Q21091190-8C620E17-F31D-4557-B910-36EB918B6B87
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21091190-8C620E17-F31D-4557-B910-36EB918B6B87
rank
NormalRank
type
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Statement
wasDerivedFrom
adedb0473adbef0025399e6d0003d0a5c5218e8d
P2860
Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.