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Q55691615-7C6AF7B5-D956-4E4E-BB2B-A2DF3D904013
Q55691615-7C6AF7B5-D956-4E4E-BB2B-A2DF3D904013
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http://www.wikidata.org/entity/statement/Q55691615-7C6AF7B5-D956-4E4E-BB2B-A2DF3D904013
Replication of genome wide association identified candidate genes confirm the role of common and rare variants in PAX7 and VAX1 in the etiology of nonsyndromic CL(P).
P2860
Q55691615-7C6AF7B5-D956-4E4E-BB2B-A2DF3D904013
BestRank
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http://www.wikidata.org/entity/statement/Q55691615-7C6AF7B5-D956-4E4E-BB2B-A2DF3D904013
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wasDerivedFrom
49533841c578cc0ea88a5cd796044f4922045bbc
P2860
VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans.