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Q38068256-271BBC57-68C7-403B-A500-383ABBE6426D
Q38068256-271BBC57-68C7-403B-A500-383ABBE6426D
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http://www.wikidata.org/entity/statement/Q38068256-271BBC57-68C7-403B-A500-383ABBE6426D
Craniosynostosis: molecular pathways and future pharmacologic therapy.
P2860
Q38068256-271BBC57-68C7-403B-A500-383ABBE6426D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38068256-271BBC57-68C7-403B-A500-383ABBE6426D
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wasDerivedFrom
b794cadf99cb546215ac9667bb89a429129dd8b9
P2860
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes