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Q56266841-0F30B91F-F968-4110-8EFA-322106B37990
Q56266841-0F30B91F-F968-4110-8EFA-322106B37990
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http://www.wikidata.org/entity/statement/Q56266841-0F30B91F-F968-4110-8EFA-322106B37990
Severe craniosynostosis with Noonan syndrome phenotype associated with SHOC2 mutation: clinical evidence of crosslink between FGFR and RAS signaling pathways
P2860
Q56266841-0F30B91F-F968-4110-8EFA-322106B37990
BestRank
Statement
http://www.wikidata.org/entity/statement/Q56266841-0F30B91F-F968-4110-8EFA-322106B37990
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wasDerivedFrom
1fda7247e895a44ed0e403941e28742ed785be32
P2860
KRAS gene mutations in Noonan syndrome familial cases cluster in the vicinity of the switch II region of the G-domain: report of another family with metopic craniosynostosis