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Q36682239-4CFC5F2E-9949-4E1E-83BA-EF5F51160C9B
Q36682239-4CFC5F2E-9949-4E1E-83BA-EF5F51160C9B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36682239-4CFC5F2E-9949-4E1E-83BA-EF5F51160C9B
Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome
P2860
Q36682239-4CFC5F2E-9949-4E1E-83BA-EF5F51160C9B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36682239-4CFC5F2E-9949-4E1E-83BA-EF5F51160C9B
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type
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wasDerivedFrom
d1f6de3a6ca3475207b9c24cd02f887a54b14664
P2860
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity.