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Q38546971-B5621809-8442-4E32-8305-F7DF0B555FD7
Q38546971-B5621809-8442-4E32-8305-F7DF0B555FD7
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http://www.wikidata.org/entity/statement/Q38546971-B5621809-8442-4E32-8305-F7DF0B555FD7
Unmasking the ciliopathies: craniofacial defects and the primary cilium.
P2860
Q38546971-B5621809-8442-4E32-8305-F7DF0B555FD7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38546971-B5621809-8442-4E32-8305-F7DF0B555FD7
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wasDerivedFrom
4c0d3b5dc4539488f9d5c0a14c29c896ee6e185a
P2860
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.