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Q24310222-8F033722-9073-4EEA-B045-D5215470DBF0
Q24310222-8F033722-9073-4EEA-B045-D5215470DBF0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24310222-8F033722-9073-4EEA-B045-D5215470DBF0
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome
P2860
Q24310222-8F033722-9073-4EEA-B045-D5215470DBF0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24310222-8F033722-9073-4EEA-B045-D5215470DBF0
rank
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wasDerivedFrom
6583cc417075c3e39b544458383410bc19556382
P2860
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis