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Q55670707-AECC2BD5-CDCF-474E-9F13-D8FEC22C5EF2
Q55670707-AECC2BD5-CDCF-474E-9F13-D8FEC22C5EF2
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http://www.wikidata.org/entity/statement/Q55670707-AECC2BD5-CDCF-474E-9F13-D8FEC22C5EF2
Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype
P2860
Q55670707-AECC2BD5-CDCF-474E-9F13-D8FEC22C5EF2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55670707-AECC2BD5-CDCF-474E-9F13-D8FEC22C5EF2
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wasDerivedFrom
492ce3a677dc719bb8e154fe6003b5da308d7370
P2860
A copy number variation morbidity map of developmental delay