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Q50459323-E2C89447-F515-4A0A-8D0F-60D1588B4B11
Q50459323-E2C89447-F515-4A0A-8D0F-60D1588B4B11
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Statement
http://www.wikidata.org/entity/statement/Q50459323-E2C89447-F515-4A0A-8D0F-60D1588B4B11
Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes.
P2860
Q50459323-E2C89447-F515-4A0A-8D0F-60D1588B4B11
BestRank
Statement
http://www.wikidata.org/entity/statement/Q50459323-E2C89447-F515-4A0A-8D0F-60D1588B4B11
rank
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type
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wasDerivedFrom
151bedd801691d45e56d923ca97a3e3dc1753d86
P2860
Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene.