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Q28293140-5C6FF2B2-098E-47E6-8DCE-6E5CF875A07B
Q28293140-5C6FF2B2-098E-47E6-8DCE-6E5CF875A07B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28293140-5C6FF2B2-098E-47E6-8DCE-6E5CF875A07B
Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse model
P2860
Q28293140-5C6FF2B2-098E-47E6-8DCE-6E5CF875A07B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28293140-5C6FF2B2-098E-47E6-8DCE-6E5CF875A07B
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wasDerivedFrom
33e8f69f1f39612d99d6c684a46d203ef6bdaa39
P2860
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome