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Q47321840-BF84B565-9DD5-4F40-894E-A7B09CB1112B
Q47321840-BF84B565-9DD5-4F40-894E-A7B09CB1112B
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Statement
http://www.wikidata.org/entity/statement/Q47321840-BF84B565-9DD5-4F40-894E-A7B09CB1112B
Clinically mild, atypical, and aged craniofacial syndrome is diagnosed as Crouzon syndrome by identification of a point mutation in the fibroblast growth factor receptor 2 gene (FGFR2).
P31
Q47321840-BF84B565-9DD5-4F40-894E-A7B09CB1112B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47321840-BF84B565-9DD5-4F40-894E-A7B09CB1112B
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wasDerivedFrom
1e3ad7ab04773123d93b497308259de3b4d7f148
P31
scholarly article