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Q36682239-1E774A84-0A2D-4355-903E-F433479906AE
Q36682239-1E774A84-0A2D-4355-903E-F433479906AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36682239-1E774A84-0A2D-4355-903E-F433479906AE
Deletions and de novo mutations of SOX11 are associated with a neurodevelopmental disorder with features of Coffin-Siris syndrome
P2860
Q36682239-1E774A84-0A2D-4355-903E-F433479906AE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36682239-1E774A84-0A2D-4355-903E-F433479906AE
rank
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type
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Statement
wasDerivedFrom
d1f6de3a6ca3475207b9c24cd02f887a54b14664
P2860
Deletion 2p25.2: a cryptic chromosome abnormality in a patient with autism and mental retardation detected using aCGH.