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Q55670707-5FB1350B-D484-43B1-8652-316A18F7C26F
Q55670707-5FB1350B-D484-43B1-8652-316A18F7C26F
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Statement
http://www.wikidata.org/entity/statement/Q55670707-5FB1350B-D484-43B1-8652-316A18F7C26F
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype
P1476
Q55670707-5FB1350B-D484-43B1-8652-316A18F7C26F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55670707-5FB1350B-D484-43B1-8652-316A18F7C26F
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type
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Statement
P1476
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype
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