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Q28249477-EC1F55C9-D9B5-4FFD-A0E0-22B2C52FEC93
Q28249477-EC1F55C9-D9B5-4FFD-A0E0-22B2C52FEC93
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28249477-EC1F55C9-D9B5-4FFD-A0E0-22B2C52FEC93
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
P31
Q28249477-EC1F55C9-D9B5-4FFD-A0E0-22B2C52FEC93
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28249477-EC1F55C9-D9B5-4FFD-A0E0-22B2C52FEC93
rank
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type
BestRank
Statement
wasDerivedFrom
023b74a55557668216637279d05b745a9b1e7086
P31
scholarly article