Reactome | Martinovic, J

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created	[InstanceEdit:2029773] Rothfels, K, 2012-01-04
dbId	2029772
displayName	Martinovic, J
firstname	Jelena
initial	J
publications	[LiteratureReference:2029812] Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome [LiteratureReference:9861705] NEK1 and DYNC2H1 are both involved in short rib polydactyly Majewski type but not in Beemer Langer cases
schemaClass	Person
surname	Martinovic

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