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Q34029106-4D0CD38C-CF71-4771-B6AC-9164FFBBC6E4
Q34029106-4D0CD38C-CF71-4771-B6AC-9164FFBBC6E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34029106-4D0CD38C-CF71-4771-B6AC-9164FFBBC6E4
A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
P2860
Q34029106-4D0CD38C-CF71-4771-B6AC-9164FFBBC6E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34029106-4D0CD38C-CF71-4771-B6AC-9164FFBBC6E4
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Statement
wasDerivedFrom
cb86f315d1e4fd5585d6a459d78b9296096a7ce1
P2860
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome