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Q36504775-A683BB80-6813-4362-9F7B-642EDB09579B
Q36504775-A683BB80-6813-4362-9F7B-642EDB09579B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36504775-A683BB80-6813-4362-9F7B-642EDB09579B
Prevalence and complications of single-gene and chromosomal disorders in craniosynostosis.
P2860
Q36504775-A683BB80-6813-4362-9F7B-642EDB09579B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36504775-A683BB80-6813-4362-9F7B-642EDB09579B
rank
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wasDerivedFrom
840dd158ff2af5d5ae8566c30e499524a9d758c7
P2860
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome