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Q34388821-02299F0A-96C2-45E9-A481-E688DA130497
Q34388821-02299F0A-96C2-45E9-A481-E688DA130497
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34388821-02299F0A-96C2-45E9-A481-E688DA130497
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome
P2860
Q34388821-02299F0A-96C2-45E9-A481-E688DA130497
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34388821-02299F0A-96C2-45E9-A481-E688DA130497
rank
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type
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Statement
wasDerivedFrom
816aedeaa36f84fc07f2d94649bfae212acef35b
P2860
Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome