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3253403
3253403
https://w3id.org/oc/corpus/br/3253403
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis
P3181
b9d84b6673d25b56a40cce0783af8c40aeb40840
P3181
Q28249477-D908647A-52BD-4C6C-8C64-93B2B76803A0
P3181
3253403
https://w3id.org/oc/corpus/br/3253403